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conventional endodontic treatment is done using two different types of sealers in the obturation to evaluate the post operative pain between the two sealers
STUDY WILL BE PERFORMED ON PATIENTS DIAGNOSED WITH SYMPTOMATIC IRREVERSABE PULPITIS.
TREATMENT PROTOCOL FOR ALL PATIENTS IS CONVENTIONAL ROOT CANAL TREATMENT
ACCESS CAVITY AND CLEANING AND SHAPING PROCEDURES WILL BE EXECUTED FOR ALL PATIENTS WITH THE SAME PROTOCOL
SELECTED PATIENTS WILL THEN BE DIVIDED INTO TWO GROUPS,
GROUP1: ALL CANALS WILL BE OBTURATED USING RESIN STANDARD SEALERS.
GROUP2: ALL CANALS WILL BE OBTURATED USING HIGH FLOW BIOCERAMIC SEALERS THAT ACCEPT WARM VERTICAL COMPACTION
POST OPERATIVE PAIN IN THE TWO GROUPS WILL BE EVALUATED USING THE VISUAL ANALOUG SCALE AND COMPARED AT DIFFERENT TIME PERIODS (12H, 24H, 48H, 72H)
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| resin group | Active Comparator | obturated with resin sealer |
|
| bio ceramic group | Active Comparator | obturated with bioceramic sealer |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| root canal sealers | Other | different sealer used in obturating root canals (resin and bio ceramic) |
|
| Measure | Description | Time Frame |
|---|---|---|
| Pain level comparison after root canal obturation with two different endodontic sealers: VAS (Visual Analogue Scale) at 12 hours | Based on the VAS (Visual Analogue Scale), the pain levels of the patients were assessed. The scale consisted of a 100-mm-long line divided into 10 equal intervals from 0 (no pain) to 100 (very severe pain). Every patient was asked to mark his or her perceived postoperative pain level on the line. | 12 hours |
| Pain level comparison after root canal obturation with two different endodontic sealers: VAS (Visual Analogue Scale) at 24 hours | Based on the VAS (Visual Analogue Scale), the pain levels of the patients were assessed. The scale consisted of a 100-mm-long line divided into 10 equal intervals from 0 (no pain) to 100 (very severe pain). Every patient was asked to mark his or her perceived postoperative pain level on the line. | 24 hours |
| Pain level comparison after root canal obturation with two different endodontic sealers: VAS (Visual Analogue Scale) at 48 hours | Based on the VAS (Visual Analogue Scale), the pain levels of the patients were assessed. The scale consisted of a 100-mm-long line divided into 10 equal intervals from 0 (no pain) to 100 (very severe pain). Every patient was asked to mark his or her perceived postoperative pain level on the line. | 48 hours |
| Pain level comparison after root canal obturation with two different endodontic sealers: VAS (Visual Analogue Scale) at 72 hours | Based on the VAS (Visual Analogue Scale), the pain levels of the patients were assessed. The scale consisted of a 100-mm-long line divided into 10 equal intervals from 0 (no pain) to 100 (very severe pain). Every patient was asked to mark his or her perceived postoperative pain level on the line. | 72 hours |
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Inclusion Criteria:
• Patients age ranges from 18-50 years old.
Exclusion Criteria:
• Teeth with immature roots
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| sara tarek mohamed, bachelor | Contact | 01007434392 | sara.alsayed@bue.edu.eg | |
| hala F khalil, lecturer | Contact | 01287595795 | hala.fayek@bue.edu.eg |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| British university in egypt | Recruiting | Cairo | 02 | Egypt |
evaluated postoperative pain results when using different sealer types in obturation
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot | Yes | No | No | Study Protocol | Dec 13, 2021 | Jan 31, 2023 | Prot_000.pdf |
| ICF | No | No | Yes | Informed Consent Form | Dec 13, 2021 | Feb 13, 2023 | ICF_001.pdf |
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| ID | Term |
|---|---|
| D010149 | Pain, Postoperative |
| ID | Term |
|---|---|
| D011183 | Postoperative Complications |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D010146 | Pain |
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randomized clinical trial
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Patients were randomly divided into two groups according to material used for obturation . each patients name will be replaced with a case number within the group to protect the privacy of medical information and data of the patients care provider and the investigator will not know the name of the patient and the assessor doesn't know the group he is assessing
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |