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Supplemental Postoperative Bupivacaine Following Non-Surgical Endodontic Treatment

StatusRecruiting
PhasePhase 2
Started
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Record status
This record was last updated April 13, 2026 (before its estimated June 30, 2026 completion). Its status may not reflect the trial's current state.

Record History

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  1. Primary completion date: Sep 30, 2025 to Jun 30, 2026
    • Primary endpoint revised
    • Study completion date: Dec 1, 2025 to Dec 31, 2026
    v3
  2. Trial status: Not Yet Recruiting to Recruitingv2 Show 5 more changesShow less
    • Primary completion date: Sep 2025 to Sep 30, 2025
    • Study completion date: Sep 2025 to Dec 1, 2025
    • Start date changed from estimate of Oct 2024 to Nov 1, 2024
    • Secondary endpoints: details revised at 2 of 2 entries
    • Site details revised
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT06655454
Lead Sponsor New York University
Conditions
(from sponsor)		 Pain Assessment, Quality of Life (QOL), Analgesic Use
Related terms Agnosia
Enrollment 150 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov