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To compare the effect of Bio-C Temp Bioceramic intracanal dressing versus calcium hydroxide as intracanal medicaments on:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Bio-C Temp | Experimental | This group will Receive Bio-C Temp Bioceramic paste as intracanal dressing |
|
| Calcium Hydroxide | Active Comparator | This group will Receive Calcium Hydroxide paste as intracanal dressing |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Bio-C Temp Intracanal Medication | Drug | Bio-C Temp Bioceramic intracanal dressing in the form of injectable premixed paste |
|
| Measure | Description | Time Frame |
|---|---|---|
| Intensity of post-operative pain | Intensity of post-operative pain as measured by Numerical Rating Scale (NRS) | 6 hours post-instrumentation |
| Intensity of post-operative pain | Intensity of post-operative pain as measured by Numerical Rating Scale (NRS) | 12 hours post-instrumentation |
| Intensity of post-operative pain | Intensity of post-operative pain as measured by Numerical Rating Scale (NRS) | 24 hours post-instrumentation |
| Intensity of post-operative pain | Intensity of post-operative pain as measured by Numerical Rating Scale (NRS) | 48 hours post-instrumentation |
| Intensity of post-operative pain | Intensity of post-operative pain as measured by Numerical Rating Scale (NRS) | 6 hours post-obturation |
| Intensity of post-operative pain | Intensity of post-operative pain as measured by Numerical Rating Scale (NRS) | 12 hours post-obturation |
| Intensity of post-operative pain | Intensity of post-operative pain as measured by Numerical Rating Scale (NRS) | 24 hours post-obturation |
| Intensity of post-operative pain |
| Measure | Description | Time Frame |
|---|---|---|
| Periapical MMP-9 level | Level Of MMP-9 Enzyme in the periapical tissue fluid, quantified by ELISA | at the first visit post- instrumentation |
| Periapical MMP-9 Level | Level of MMP-9 enzyme in the periapical tissue fluid, Quantified by ELISA |
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Inclusion Criteria:
Age between 18-50 years old.
Males and females.
Healthy patients categorized as I or II according to The American Society of Anesthesiologists.
(ASA I or II), with no underlying allergies.
Single-rooted mandibular premolar teeth, having single root canal:
Patients accepting to participate in the trial.
Patients who can understand pain scale and can sign the informed consent
Exclusion Criteria:
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| Calcium Hydroxide Intracanal medication | Drug | Calcium Hydroxide intracanal dressing in the form of injectable premixed paste |
|
Intensity of post-operative pain as measured by Numerical Rating Scale (NRS) |
| 48 hours post-obturation |
| After 1 week at the second visit (pre-obturation) |
| ID | Term |
|---|---|
| D010485 | Periapical Periodontitis |
| D010149 | Pain, Postoperative |
| ID | Term |
|---|---|
| D010483 | Periapical Diseases |
| D007571 | Jaw Diseases |
| D009057 | Stomatognathic Diseases |
| D010510 | Periodontal Diseases |
| D009059 | Mouth Diseases |
| D010518 | Periodontitis |
| D011183 | Postoperative Complications |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D010146 | Pain |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
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