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RECRUITING
NCT06585540
PHASE3

A Pilot Study to Evaluate Barhemsys for the Prevention of Postoperative Nausea And Vomiting in the Bariatric Surgery Population

Sponsor: Benaroya Research Institute

View on ClinicalTrials.gov

Summary

To assess the effectiveness of Amisulpride to treat Post Operative Nausea and Vomiting (PONV) and to assess the effectiveness of Amisulpride to prevent PONV following bariatric surgery.

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2024-09-13

Completion Date

2026-01

Last Updated

2024-09-26

Healthy Volunteers

Yes

Interventions

DRUG

Amisulpride IV Prevention

Patients in this arm will receive Amisulpride 5mg IV as a preventative dose after the induction of anesthesia

DRUG

Amisulpride IV Treatment

Patients in this arm will receive Amisulpride 10mg IV for first-line treatment of Post-Operative Nausea and Vomiting in the post-anesthesia care unit.

DRUG

Placebo Preventative

Patients in this arm will receive placebo (Normal Saline) while under general anesthesia

DRUG

Placebo Treatment

Patients in this Arm will receive placebo as first line treatment of Post-Operative Nausea and Vomiting in the Post Anesthesia Care Unit

Locations (1)

Virginia Mason Medical Center

Seattle, Washington, United States