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| ID | Type | Description | Link |
|---|---|---|---|
| 815642 | Other Identifier | University of Pennsylvania IRB |
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The intent of this study is to evaluate the clinical performance of an experimental dental bonding agent for use with dental restorative composites with and without pretreatment of the tooth dentin and enamel using phosphoric acid etching.
The intent of this study is to evaluate the clinical performance of an experimental dental bonding agent (adhesive) for use with dental restorative composites with and without pretreatment of the tooth dentin and enamel using phosphoric acid etching.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Adhesive without acid pretreatment | Experimental | Experimental adhesive w/out phosphoric acid in post. rest. |
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| Adhesive with acid pretreatment | Active Comparator | Experimental adhesive with phosphoric acid in post. rest. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Experimental adhesive w/out phosphoric acid in post. rest. | Device | Experimental adhesive without phosphoric acid in posterior restorations |
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| Measure | Description | Time Frame |
|---|---|---|
| Color Match | The color match will be assessed clinically according to Ryge (1973)* for matching with adjacent teeth and stability of color matching over time. Assessments will be done to the following criteria: Alpha= Restoration matches adjacent tooth structure in shade and/or translucency. Bravo= Mismatch in shade and/or translucency is within normal range of tooth shades. Charlie= Mismatch in shade and/or translucency is outside normal range of tooth shades. *As per the Investigation Protocol, United States Public Health Service (USPHS) direct evaluation procedures were conducted using modified methods reported by Ryge in 1973. As described by Ryge in 1973, the term "clinical assessment" means a visual examination by a dentist, using a mouth mirror, an explorer, and supplementary lighting as needed. | Baseline, 6 months, 18 months; Note: The 36 month evaluation was an option in the protocol at the time of investigation initiation. The study was concluded at 18 months. Thus 36 month data does not exist. |
| Marginal Discoloration | Marginal discoloration will be assessed clinically according to Ryge (1973)* over time. Assessments will be done to the following criteria: Alpha= No visual evidence of marginal discoloration. Bravo= Marginal discoloration present but has not penetrated in a pulpal direction. Charlie= Marginal discoloration has penetrated in a pulpal direction. *As per the Investigation Protocol, United States Public Health Service (USPHS) direct evaluation procedures were conducted using modified methods reported by Ryge in 1973. As described by Ryge in 1973, the term "clinical assessment" means a visual examination by a dentist, using a mouth mirror, an explorer, and supplementary lighting as needed. | Baseline, 6 months, 18 months. Note: The 36 month evaluation was an option in the protocol at the time of investigation initiation. The study was concluded at 18 months. Thus 36 month data does not exist. |
| Marginal Integrity | Change in marginal integrity will be assessed clinically according to Ryge (1973)* over time. Assessments will be done to the following criteria: A= Explorer does not catch or slight catch with no visible crevice. B= Explorer catches and crevice is visible but no exposure of dentin or base. C= Explorer penetrates crevice and defect extended to amelo-dentinal junction. D= Restoration is fractured, mobile, or missing in part or in toto. *As per the Investigation Protocol, United States Public Health Service (USPHS) direct evaluation procedures were conducted using modified methods reported by Ryge in 1973. As described by Ryge in 1973, the term "clinical assessment" means a visual examination by a dentist, using a mouth mirror, an explorer, and supplementary lighting as needed. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Ricardo Walter, DDS | University of Pennsylvania | Principal Investigator |
| Alan M. Atlas, DMD | Academy House of Professional Offices | Principal Investigator |
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| ID | Title | Description |
|---|---|---|
| FG000 | Experimental Adhesive w/Out Phosphoric Acid in Posterior Restoration | Experimental adhesive without phosphoric acid in posterior restoration |
| FG001 | Experimental Adhesive w/ Phosphoric Acid in Post Restoration | Experimental adhesive with phosphoric acid in post restoration |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
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Note: The units analyzed are teeth and most participants had more than one tooth treated in this study. A same participant could have individual teeth assigned to either arm. Most participants had teeth counted in both arms. A participant could have up to 4 units (teeth) treated and each unit was randomly assigned to one of the two arms.
Participants were randomized to exclude bias due to age and sex.
| ID | Title | Description |
|---|---|---|
| BG000 | Experimental: Adhesive With and Without Acid Pretreatment | Experimental adhesive with and without phosphoric acid in posterior restoration |
| Units | Counts |
|---|---|
| Participants |
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| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Patients were between 18 and 65 years of age. No additional information was recorded regarding patient age. |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Color Match | The color match will be assessed clinically according to Ryge (1973)* for matching with adjacent teeth and stability of color matching over time. Assessments will be done to the following criteria: Alpha= Restoration matches adjacent tooth structure in shade and/or translucency. Bravo= Mismatch in shade and/or translucency is within normal range of tooth shades. Charlie= Mismatch in shade and/or translucency is outside normal range of tooth shades. *As per the Investigation Protocol, United States Public Health Service (USPHS) direct evaluation procedures were conducted using modified methods reported by Ryge in 1973. As described by Ryge in 1973, the term "clinical assessment" means a visual examination by a dentist, using a mouth mirror, an explorer, and supplementary lighting as needed. | This is the total number of participants remaining at the end of the study who completed the 18 month follow-up. 22 participants presented for the 18 month evaluation. Most participants had subject teeth in both arms of the study. The reporting below is on the number of teeth, not subjects. | Posted | Number | teeth | Baseline, 6 months, 18 months; Note: The 36 month evaluation was an option in the protocol at the time of investigation initiation. The study was concluded at 18 months. Thus 36 month data does not exist. | teeth | teeth |
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Adverse Events | Intervention was the use of phosphoric acid. In the experimental group phosphoric acid was used. In the control group, phosphoric acid was not used. Dosage: As visually needed to cover exposed dentin and prepared enamel. Frequency: Once, at placement of filling |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Ricardo Walter | University of Pennslyvania | 215-898-9164 | walterr@dental.upenn.edu |
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| ID | Term |
|---|---|
| D003731 | Dental Caries |
| ID | Term |
|---|---|
| D017001 | Tooth Demineralization |
| D014076 | Tooth Diseases |
| D009057 | Stomatognathic Diseases |
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| Experimental adhesive with phosphoric acid in post. rest. | Device | Experimental adhesive with phosphoric acid in posterior restorations |
|
| Baseline, 6 months, 18 months. Note: The 36 month evaluation was an option in the protocol at the time of investigation initiation. The study was concluded at 18 months. Thus 36 month data does not exist. |
| Presence of Secondary Dental Caries (Cavities) | Change in presence of secondary dental caries will be assessed clinically according to Ryge (1973)* over time. Assessments will be done to the following criteria: A= No caries present. D= Caries present associated with the restoration. *As per the Investigation Protocol, United States Public Health Service (USPHS) direct evaluation procedures were conducted using modified methods reported by Ryge in 1973. As described by Ryge in 1973, the term "clinical assessment" means a visual examination by a dentist, using a mouth mirror, an explorer, and supplementary lighting as needed. Note: Secondary caries is a categorical, dichotomous variable, i.e. there is caries or not. This was assessed clinically and radiographically by a trained professional (dentist). | Baseline, 6 months, 18 months; Note: The 36 month evaluation was an option in the protocol at the time of investigation initiation. The study was concluded at 18 months. Thus 36 month data does not exist. |
| Presence of Restoration Fractures (Localized or Bulk) | The restoration will be assessed clinically according to Ryge (1973)* for presence of fractures over time. Assessments will be done to the following criteria: A= Smooth restoration surface with no irregularities. B= Slightly rough or pitted restoration surface. Can be refinished. C= Deeply pitted or grooved (not related to anatomy) restoration finish. Can not be refinished. D= Restoration surface is fractured or flaking. *As per the Investigation Protocol, United States Public Health Service (USPHS) direct evaluation procedures were conducted using modified methods reported by Ryge in 1973. As described by Ryge in 1973, the term "clinical assessment" means a visual examination by a dentist, using a mouth mirror, an explorer, and supplementary lighting as needed. | Baseline, 6 months, 18 months; Note: The 36 month evaluation was an option in the protocol at the time of investigation initiation. The study was concluded at 18 months. Thus 36 month data does not exist. |
| Post-operative Sensitivity | Patient will be interviewed to assess post-operative sensitivity according to the following criteria: A= No sensitivity. B= Mild sensitivity. C= Moderate sensitivity with no restoration replacement required. D= Sever sensitivity. Replacement of restoration is required. Tooth sensitivity will be assessed at baseline and each follow-up appointment using cold thermal test (Endo-Ice, Hygienic) and Electric Pulp Test (EPT) when indicated. | Baseline, 6 months, 18 months; Note: The 36 month evaluation was an option in the protocol at the time of investigation initiation. The study was concluded at 18 months. Thus 36 month data does not exist. |
| Surface Condition of Restoration | The change in surface condition of restoration will be assessed clinically according to Ryge (1973)* over time. Assessments will be done to the following criteria: A= Restoration is continuous with existing anatomic form. B= Restoration is discontinuous with existing anatomic form but missing material is not sufficient to expose dentin or lining. C= Sufficient restorative material is lost to expose dentin. *As per the Investigation Protocol, United States Public Health Service (USPHS) direct evaluation procedures were conducted using modified methods reported by Ryge in 1973. As described by Ryge in 1973, the term "clinical assessment" means a visual examination by a dentist, using a mouth mirror, an explorer, and supplementary lighting as needed. | Baseline, 6 months, 18 months; Note: The 36 month evaluation was an option in the protocol at the time of investigation initiation. The study was concluded at 18 months. Thus 36 month data does not exist. |
| Gingival Inflammation Index | Patient's gingiva will be assessed clinically according to Ryge (1973)* over time. Assessments will be done to the following criteria: 0 = Normal gingiva.
Note: At 6 months data was not reported. At Baseline, all patients presented a score of 0. Any patient with a score greater than zero would have been excluded at baseline. Patients who received Class I restorations were not assessed as these restorations are limited to the chewing surface and not related to the health of gums. | 18 months; Note: The 36 month evaluation was an option in the protocol at the time of investigation initiation. The study was concluded at 18 months. Thus 36 month data does not exist. |
| teeth |
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| Count of Units |
| teeth |
| teeth |
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| Sex/Gender, Customized | Number | participants | Participants |
|
| Region of Enrollment | Number | participants | Participants |
|
| ID | Title | Description |
|---|---|---|
| OG000 | Experimental Adhesive w/Out Phosphoric Acid in Posterior Restoration (Baseline) | Experimental adhesive without phosphoric acid in posterior restoration (Baseline) |
| OG001 | Experimental Adhesive w/ Phosphoric Acid in Posterior Restoration (Baseline) | Experimental adhesive with phosphoric acid in posterior restoration (Baseline) |
| OG002 | Experimental Adhesive w/Out Phosphoric Acid in Posterior Restoration (6-month) | Experimental adhesive without phosphoric acid in posterior restoration (6-month) |
| OG003 | Experimental Adhesive w/ Phosphoric Acid in Posterior Restoration (6-month) | Experimental adhesive with phosphoric acid in posterior restoration (6-month) |
| OG004 | Experimental Adhesive w/Out Phosphoric Acid in Posterior Restoration (18-month) | Experimental adhesive without phosphoric acid in posterior restoration (18-month) |
| OG005 | Experimental Adhesive w Phosphoric Acid in Posterior Restoration (18-month) | Experimental adhesive with phosphoric acid in posterior restoration (18-month) |
|
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| Primary | Marginal Discoloration | Marginal discoloration will be assessed clinically according to Ryge (1973)* over time. Assessments will be done to the following criteria: Alpha= No visual evidence of marginal discoloration. Bravo= Marginal discoloration present but has not penetrated in a pulpal direction. Charlie= Marginal discoloration has penetrated in a pulpal direction. *As per the Investigation Protocol, United States Public Health Service (USPHS) direct evaluation procedures were conducted using modified methods reported by Ryge in 1973. As described by Ryge in 1973, the term "clinical assessment" means a visual examination by a dentist, using a mouth mirror, an explorer, and supplementary lighting as needed. | This is the total number of participants remaining at the end of the study who completed the 18 month follow-up. 22 participants presented for the 18 month evaluation. Most participants had subject teeth in both arms of the study. The reporting below is on the number of teeth, not subjects. | Posted | Number | teeth | Baseline, 6 months, 18 months. Note: The 36 month evaluation was an option in the protocol at the time of investigation initiation. The study was concluded at 18 months. Thus 36 month data does not exist. | teeth | teeth |
|
|
|
| Primary | Marginal Integrity | Change in marginal integrity will be assessed clinically according to Ryge (1973)* over time. Assessments will be done to the following criteria: A= Explorer does not catch or slight catch with no visible crevice. B= Explorer catches and crevice is visible but no exposure of dentin or base. C= Explorer penetrates crevice and defect extended to amelo-dentinal junction. D= Restoration is fractured, mobile, or missing in part or in toto. *As per the Investigation Protocol, United States Public Health Service (USPHS) direct evaluation procedures were conducted using modified methods reported by Ryge in 1973. As described by Ryge in 1973, the term "clinical assessment" means a visual examination by a dentist, using a mouth mirror, an explorer, and supplementary lighting as needed. | This is the total number of participants remaining at the end of the study who completed the 18 month follow-up. 22 participants presented for the 18 month evaluation. Most participants had subject teeth in both arms of the study. The reporting below is on the number of teeth, not subjects. | Posted | Number | teeth | Baseline, 6 months, 18 months. Note: The 36 month evaluation was an option in the protocol at the time of investigation initiation. The study was concluded at 18 months. Thus 36 month data does not exist. | teeth | teeth |
|
|
|
| Primary | Presence of Secondary Dental Caries (Cavities) | Change in presence of secondary dental caries will be assessed clinically according to Ryge (1973)* over time. Assessments will be done to the following criteria: A= No caries present. D= Caries present associated with the restoration. *As per the Investigation Protocol, United States Public Health Service (USPHS) direct evaluation procedures were conducted using modified methods reported by Ryge in 1973. As described by Ryge in 1973, the term "clinical assessment" means a visual examination by a dentist, using a mouth mirror, an explorer, and supplementary lighting as needed. Note: Secondary caries is a categorical, dichotomous variable, i.e. there is caries or not. This was assessed clinically and radiographically by a trained professional (dentist). | This is the total number of participants remaining at the end of the study who completed the 18 month follow-up. 22 participants presented for the 18 month evaluation. Most participants had subject teeth in both arms of the study. The reporting below is on the number of teeth, not subjects. | Posted | Number | teeth | Baseline, 6 months, 18 months; Note: The 36 month evaluation was an option in the protocol at the time of investigation initiation. The study was concluded at 18 months. Thus 36 month data does not exist. | teeth | teeth |
|
|
|
| Primary | Presence of Restoration Fractures (Localized or Bulk) | The restoration will be assessed clinically according to Ryge (1973)* for presence of fractures over time. Assessments will be done to the following criteria: A= Smooth restoration surface with no irregularities. B= Slightly rough or pitted restoration surface. Can be refinished. C= Deeply pitted or grooved (not related to anatomy) restoration finish. Can not be refinished. D= Restoration surface is fractured or flaking. *As per the Investigation Protocol, United States Public Health Service (USPHS) direct evaluation procedures were conducted using modified methods reported by Ryge in 1973. As described by Ryge in 1973, the term "clinical assessment" means a visual examination by a dentist, using a mouth mirror, an explorer, and supplementary lighting as needed. | This is the total number of participants remaining at the end of the study who completed the 18 month follow-up. 22 participants presented for the 18 month evaluation. Most participants had subject teeth in both arms of the study. The reporting below is on the number of teeth, not subjects. | Posted | Number | teeth | Baseline, 6 months, 18 months; Note: The 36 month evaluation was an option in the protocol at the time of investigation initiation. The study was concluded at 18 months. Thus 36 month data does not exist. | teeth | teeth |
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|
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| Primary | Post-operative Sensitivity | Patient will be interviewed to assess post-operative sensitivity according to the following criteria: A= No sensitivity. B= Mild sensitivity. C= Moderate sensitivity with no restoration replacement required. D= Sever sensitivity. Replacement of restoration is required. Tooth sensitivity will be assessed at baseline and each follow-up appointment using cold thermal test (Endo-Ice, Hygienic) and Electric Pulp Test (EPT) when indicated. | This is the total number of participants remaining at the end of the study who completed the 18 month follow-up. 22 participants presented for the 18 month evaluation. Most participants had subject teeth in both arms of the study. The reporting below is on the number of teeth, not subjects. | Posted | Number | teeth | Baseline, 6 months, 18 months; Note: The 36 month evaluation was an option in the protocol at the time of investigation initiation. The study was concluded at 18 months. Thus 36 month data does not exist. | teeth | teeth |
|
|
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| Primary | Surface Condition of Restoration | The change in surface condition of restoration will be assessed clinically according to Ryge (1973)* over time. Assessments will be done to the following criteria: A= Restoration is continuous with existing anatomic form. B= Restoration is discontinuous with existing anatomic form but missing material is not sufficient to expose dentin or lining. C= Sufficient restorative material is lost to expose dentin. *As per the Investigation Protocol, United States Public Health Service (USPHS) direct evaluation procedures were conducted using modified methods reported by Ryge in 1973. As described by Ryge in 1973, the term "clinical assessment" means a visual examination by a dentist, using a mouth mirror, an explorer, and supplementary lighting as needed. | This is the total number of participants remaining at the end of the study who completed the 18 month follow-up. 22 participants presented for the 18 month evaluation. Most participants had subject teeth in both arms of the study. The reporting below is on the number of teeth, not subjects. | Posted | Number | teeth | Baseline, 6 months, 18 months; Note: The 36 month evaluation was an option in the protocol at the time of investigation initiation. The study was concluded at 18 months. Thus 36 month data does not exist. | teeth | teeth |
|
|
|
| Primary | Gingival Inflammation Index | Patient's gingiva will be assessed clinically according to Ryge (1973)* over time. Assessments will be done to the following criteria: 0 = Normal gingiva.
Note: At 6 months data was not reported. At Baseline, all patients presented a score of 0. Any patient with a score greater than zero would have been excluded at baseline. Patients who received Class I restorations were not assessed as these restorations are limited to the chewing surface and not related to the health of gums. | This is the total number of participants remaining at the end of the study who completed the 18 month follow-up. 22 participants presented for the 18 month evaluation. Most participants had subject teeth in both arms of the study. The reporting below is on the number of teeth, not subjects. Twenty-two (22) of the restorations were Class I and have no interaction with the gingival tissue and therefore were not scored. Scores below are for the remaining 42 Class II restorations. | Posted | Number | teeth | 18 months; Note: The 36 month evaluation was an option in the protocol at the time of investigation initiation. The study was concluded at 18 months. Thus 36 month data does not exist. | teeth | teeth |
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| 0 |
| 37 |
| 0 |
| 37 |
| 0 |
| 37 |
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| 2 |
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