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Efficacy of Buprenorphine on Postoperative Endodontic Analgesia (EBPEA)

University Hospitals (UH) logo

University Hospitals (UH)

Status and phase

Terminated
Phase 1

Conditions

Postoperative Pain

Treatments

Drug: Sterile saline
Drug: lidocaine, epinephrine (Local anesthetic)
Drug: Buprenorphine

Study type

Interventional

Funder types

Other

Identifiers

NCT03268278
UHClevelandMCBupStudy

Details and patient eligibility

About

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

Enrollment

10 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 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 criteria

  • pregnancy, allergy to buprenorphine, allergy to local anesthetic

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

10 participants in 2 patient groups, including a placebo group

buprenorphine and local anesthetic
Active Comparator group
Description:
buprenorphine added to local anesthetic
Treatment:
Drug: Buprenorphine
Drug: lidocaine, epinephrine (Local anesthetic)
sterile saline and local anesthetic
Placebo Comparator group
Description:
sterile saline (placebo) added to local anesthetic
Treatment:
Drug: lidocaine, epinephrine (Local anesthetic)
Drug: Sterile saline

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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