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RCT to Test Regional Anesthesia Effect on Decreased Opiate Use

NCT06989866 · Status: ENROLLING_BY_INVITATION · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2025-10-09

No results posted yet for this study

Summary

Examining use of strong pain medication with the use of perioperative anesthetic medications vs no use of the same perioperative medication

Conditions

  • Postoperative Pain

Interventions

DRUG

Bupivacaine

Bupivicaine injection post operatively

DRUG

Saline (NaCl 0,9 %) (placebo)

Saline injected to control group

Sponsors & Collaborators

  • United States Naval Medical Center, Portsmouth

    lead FED

Principal Investigators

  • Tokunbo I Ayeni, MD · United States Naval Medical Center, Portsmouth

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-12-01
Primary Completion
2026-08-01
Completion
2026-09-01
FDA Drug
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06989866 on ClinicalTrials.gov