Status:
TERMINATED
Efficacy of Buprenorphine on Postoperative Endodontic Analgesia
Lead Sponsor:
University Hospitals Cleveland Medical Center
Conditions:
Postoperative Pain
Eligibility:
All Genders
18+ years
Phase:
PHASE1
Brief Summary
To see whether the addition of buprenorphone to local anesthesia will lengthen postoperative analgesia for endodontic pain
Eligibility Criteria
Inclusion
- persons with preoperative pain to percussion of a tooth with pulpal disease requiring endodontic therapy, healthy individuals, ASA Class I and II, no known allergies to the drugs being administered
Exclusion
- pregnancy, allergy to buprenorphine, allergy to local anesthetic
Key Trial Info
Start Date :
April 1 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 1 2018
Estimated Enrollment :
10 Patients enrolled
Trial Details
Trial ID
NCT03268278
Start Date
April 1 2017
End Date
July 1 2018
Last Update
April 23 2019
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
University Hospitals Cleveland Medical Center
Cleveland, Ohio, United States, 44106