Efficacy of Buprenorphine on Postoperative Endodontic Analgesia

Stopped early · Phase 1 · Has a placebo group

Conditions studied: Postoperative Pain

In brief

To see whether the addition of buprenorphone to local anesthesia will lengthen postoperative analgesia for endodontic pain

Key facts

Study ID

NCT03268278

Run by

University Hospitals Cleveland Medical Center

People needed

10

Starts

2017-04-01

Expected to finish

2018-07-01

Last updated by the study team

2019-04-23

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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

You may not qualify if…

• pregnancy, allergy to buprenorphine, allergy to local anesthetic

Where it is running

• University Hospitals Cleveland Medical Center — Cleveland, Ohio, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.