Postoperative Pain Clinical Trial
Official title:
The Effect of Different Obturation Techniques on Postobturation Pain in Single-Visit Root Canal Treatment: A Prospective Clinical Randomized Study
NCT number | NCT06146894 |
Other study ID # | HA2427 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | December 1, 2023 |
Est. completion date | June 28, 2024 |
The goal of this prospective clinical randomized study is to evaluate the effect of different obturation techniques on postobturation pain in single-visit root canal treatment in 18-60 years old patient who present no systemic disease (American Society of Anesthesiology class I or II) and require nonsurgical root canal treatment The main question it aims to answer which obturation technique used with bioceramic sealer cause less postobturation pain in single-visit root canal treatment in comparison to AH plus sealer used with lateral condensation or warm vertical compaction. Participants will receive single visit root canal treatment using bioceramic sealer with different obturation techniques Group 1: Single cone technique Group 2: lateral condensation technique Group 3: Vertical compaction technique to see effect of different obturation technique on postobturation pain in single-visit root canal treatment.
Status | Recruiting |
Enrollment | 150 |
Est. completion date | June 28, 2024 |
Est. primary completion date | June 10, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility | Inclusion Criteria: - Patients aged 18-60 years who presented no systemic disease (American Society of Anesthesiology class I or II) and required nonsurgical root canal treatment. - Diagnosis of asymptomatic irreversible pulpitis in a molar tooth with 3 independent root canals. Exclusion Criteria: - Presence of immature root apexes, root fracture, or periodontal disease - Use of any analgesic, anti- inflammatory, or antibiotics before the treatment. |
Country | Name | City | State |
---|---|---|---|
Egypt | kafrelsheikh University | Kafr Ash Shaykh | Kafr El-Shaikh |
Lead Sponsor | Collaborator |
---|---|
Kafrelsheikh University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | postobturation pain | Presence of post-obturation pain will accessed by visual analog scale (VAS) scale (0-10), where 0 showed no pain, 1-3 mild pain, 4-6 moderate pain, 7-9 severe pain, and 10 worst possible pain. | 30 days |
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