Trials / Completed
CompletedNCT04326998
Gutta-percha Solvent on Postoperative Pain After Root Canal Retreatment
Natural Gutta-percha Solvent Did Not Affect Postoperative Pain in Retreatment: a Randomized Clinical Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (actual)
- Sponsor
- Mahidol University · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The process of non-surgical retreatment includes removing the previous root canal filling materials, disinfecting and sealing the root canal system to prevent re-infection. Gutta-percha is the most common root canal filling material used with various types of sealers. To remove gutta-percha, solvent has been suggested because of its ability to dissolve gutta-percha. The new formula, under the brand name, GuttaClear, has been investigated for its comparable dissolving ability and lower cytotoxicity when compared with others that are currently used. However, no information is currently available of GuttaClear solvent concerning postoperative pain. Therefore, the present study will evaluate postoperative pain after non-surgical retreatment cases using GuttaClear as a solvent compared with no solvent used. Sixty participants are chosen and distributed into 2 groups, randomly. After the procedures, participants will receive the questionnaires about postoperative pain and the amount of medication intake. Both will be recorded at six time periods: (1) immediately after procedure; (2) 6 hours after procedure; (3) 12 hours after procedure; (4) 24 hours after procedure; (5) 48 hours after procedure and (6) 72 hours after procedure.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | solvent | using solvent (GuttaClear) in procedure |
| PROCEDURE | non-solvent | non-solvent |
Timeline
- Start date
- 2019-09-18
- Primary completion
- 2021-03-18
- Completion
- 2021-06-18
- First posted
- 2020-03-30
- Last updated
- 2021-09-21
Locations
1 site across 1 country: Thailand
Source: ClinicalTrials.gov record NCT04326998. Inclusion in this directory is not an endorsement.