← Eichor
Study identifier: NCT06655454 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Supplemental Postoperative Bupivacaine Following Non-Surgical Endodontic Treatment

Condition: Pain Assessment · Quality of Life (QOL) · Analgesic Use  ·  Sponsor: New York University

PhasePhase 2
Planned participants150
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The study will investigate the impact of an additional injection of long-acting anesthetic on pain level, quality of life, and use of pain medication after a nonsurgical endodontic treatment. The long-acting anesthetic will be compared to a mock injection group and a group with no additional anesthetic to determine any differences in effects.

This description comes directly from the study's public registry record.

Talk to the study team

Lorel E Burns, DDS  ·  212-998-9332  ·  leb409@nyu.edu

NYUSOM IRB  ·  212-263-4110  ·  irb-info@nyulangone.org

Always discuss trial participation with your own doctor first.

Locations (1)

New York University College of DentistryNew York, New York, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06655454