Actively Recruiting

Phase 2
Age: 18Years - 79Years
FEMALE
Healthy Volunteers
NCT06488001

Preoperative Use of Pantoprazole for Prevention of Post Operative Nausea and Vomiting in Gynecologic Surgery

Led by United States Naval Medical Center, Portsmouth · Updated on 2025-05-21

132

Participants Needed

1

Research Sites

222 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to see if pantoprazole (a proton pump inhibitor used for acid reflux/heart burn) can reduce nausea and vomiting after gynecologic surgery in women between the ages of 18 and 79. Researchers will compare a placebo to the active medication. Participants will be asked to take three pills around their surgery, two taken before and one taken the night after.

CONDITIONS

Official Title

Preoperative Use of Pantoprazole for Prevention of Post Operative Nausea and Vomiting in Gynecologic Surgery

Who Can Participate

Age: 18Years - 79Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Women aged 18 to 79 years
  • Undergoing elective gynecological surgery by open abdominal, endoscopic, or vaginal approach
  • Surgery performed under general anesthesia
Not Eligible

You will not qualify if you...

  • Pregnant women
  • Patients with gastrointestinal disease needing ongoing medical treatment
  • History of gastrointestinal surgery except diagnostic procedures, appendectomy, or cholecystectomy
  • Use of H2 receptor blockers, proton pump inhibitors, or GERD therapy within 30 days before surgery
  • History of postoperative nausea and vomiting requiring extra prevention measures
  • Known or suspected malignancy
  • Lactose intolerance

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Naval Medical Center Portsmouth

Portsmouth, Virginia, United States, 23708

Actively Recruiting

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Research Team

C

Casey Timmerman, DO

CONTACT

M

Melissa Infosino, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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