Actively Recruiting

Phase 4
Age: 21Years - 65Years
FEMALE
NCT07101250

Preoperative Acetazolamide

Led by Prisma Health-Upstate · Updated on 2026-02-20

100

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this randomized study looks at whether giving patients a medicine called acetazolamide (also called Diamox) before they have laparoscopic hysterectomy may decrease postoperative pain. Researchers will compare acetazolamide to a placebo or inactive drug, to see if acetazolamide helps the pain that may occur after surgery from the gas used in the abdomen during the laparoscopic procedure. Patients will be asked to rate their pain before surgery and after surgery through 24 hours.

CONDITIONS

Official Title

Preoperative Acetazolamide

Who Can Participate

Age: 21Years - 65Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Female participants
  • Ages 21 to 65 years
  • Undergoing total laparoscopic hysterectomy (TLH) for benign indications with or without bilateral salpingoophorectomy
  • Undergoing total laparoscopic hysterectomy (TLH) for benign indications with or without cystoscopy
Not Eligible

You will not qualify if you...

  • Allergy to acetazolamide or sulfonamides
  • Known electrolyte disturbances
  • Pregnancy
  • Kidney failure or creatinine greater than 1.5
  • Use of diuretics or lithium
  • Chronic obstructive pulmonary disease (COPD) or other lung diseases
  • Central nervous system disorders
  • Liver disease
  • Glaucoma
  • Preoperative or chronic opioid use
  • Diagnosis of fibromyalgia
  • Preoperative shoulder pain
  • Conversion to laparotomy during surgery
  • Intraoperative bladder or bowel injury
  • Inability to understand or use the visual analog scale
  • Undergoing concurrent reconstructive procedures

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

Prisma Health

Greenville, South Carolina, United States, 29605

Actively Recruiting

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Research Team

P

Patti Parker, BSN

CONTACT

P

Paul Miller, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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