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NCT06655454

Supplemental Postoperative Bupivacaine Following Non-Surgical Endodontic Treatment

Recruiting now Phase 2 Last updated 13 April 2026
What this trial tests

Phase 2 trial testing Supplemental Postoperative Bupivacaine in Pain Assessment in 150 participants. Currently enrolling.

Timeline
1 November 2024
Primary endpoint
30 June 2026
31 December 2026

Quick facts

Lead sponsorNew York University
PhasePhase 2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposesupportive care
Enrollment150
Start date1 November 2024
Primary completion30 June 2026
Estimated completion31 December 2026
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

New York University

Who can join

18 and older, any sex, with Pain Assessment or Quality of Life (QOL). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Pain Assessment

Currently open trials in the same condition.

Other New York University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06655454.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing