Actively Recruiting

Phase 2
Age: 18Years - 65Years
FEMALE
Healthy Volunteers
NCT06483659

Intravenous Oxytocin for Post Operative Pain After Minimally Invasive Hysterectomy

Led by Brigham and Women's Hospital · Updated on 2025-12-30

152

Participants Needed

1

Research Sites

78 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a randomized, double-blinded, placebo-controlled trial to compare the effectiveness of IV oxytocin infusion to placebo on peri-operative opioid consumption and reducing post-operative pain following a minimally invasive hysterectomy under general anesthesia.

CONDITIONS

Official Title

Intravenous Oxytocin for Post Operative Pain After Minimally Invasive Hysterectomy

Who Can Participate

Age: 18Years - 65Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Ages 18-65 years old
  • ASA category 1-3
  • Scheduled to undergo minimally invasive hysterectomy
  • No documented allergy to oxytocin
Not Eligible

You will not qualify if you...

  • ASA category 4 or greater
  • Age over 65 years old
  • Additional surgical procedures such as laparotomy, omentectomy, cystectomy, vaginectomy, or endometriosis ablation
  • Active opioid use exceeding 10 mg oxycodone per day
  • Opioid use disorder or current treatment with naltrexone or Suboxone
  • Allergies to acetaminophen, celecoxib, ketorolac, fentanyl, hydromorphone, or oxycodone
  • Use of epidural or regional anesthesia for pain management
  • Inability to understand questionnaires
  • Surgery converted to open or extended procedure
  • Intra-operative blood loss over 500 ml
  • Epidural catheter placement or regional anesthesia in PACU
  • Hospitalization due to surgical or anesthetic complications

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

Brigham and Women's Hospital

Boston, Massachusetts, United States, 02215

Actively Recruiting

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Research Team

J

John J. Kowalczyk, MD

CONTACT

R

Rusul I Al-Ani

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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