drugset / Trial / NCT06002152

Superficial Cervical Plexus Block and Quality of Recovery After Thyroidectomy

NCT06002152

Phase 2 Completed 160 enrolled Yale University
RandomizedParallel-groupQuadruple-blindSupportive care

Summary

The goal of this clinical trial is to learn whether a superficial cervical plexus block improves quality of recovery after thyroid surgery. Investigators will compare a superficial cervical plexus block with bupivacaine compared to an identical procedure performed saline placebo to see if there is a difference in quality of recovery on the first postoperative day. The main question to answer is: • Does a superficial cervical plexus block with bupivacaine compared to placebo improve quality of recovery in patients having thyroid surgery. Participants will: * Fill out an initial preoperative survey * Be randomized to receive a superficial cervical plexus block with bupivacaine or saline placebo while under anesthesia before the surgery starts * Fill out a survey about recovery on the first day after surgery

Timeline

Start
2023-11-27
Primary completion
2026-02-03
Completion
2026-02-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Bupivacaine Other / unclassified 0.25 % Other
Subject Bupivacaine Other / unclassified 10 ml Other

Indications

No indication recorded.