Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
FEMALE
NCT06837506

Ultrasound Guided Rectus Sheath Block Versus Intrathecal Morphine for Postoperative Analgesia in Patients Undergoing Open Total Abdominal Hysterectomy

Led by Ain Shams University · Updated on 2025-02-21

80

Participants Needed

1

Research Sites

23 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to compare the effectiveness and safety of ultrasound-guided rectus sheath block versus intrathecal morphine for postoperative analgesia in patients undergoing open total abdominal hysterectomy.

CONDITIONS

Official Title

Ultrasound Guided Rectus Sheath Block Versus Intrathecal Morphine for Postoperative Analgesia in Patients Undergoing Open Total Abdominal Hysterectomy

Who Can Participate

Age: 18Years - 65Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 65 years old
  • American Society of Anesthesiologists (ASA) physical status I or II
  • Undergoing open total abdominal hysterectomy
Not Eligible

You will not qualify if you...

  • Having liver, kidney, or heart disease
  • Known allergy to local anesthetics
  • Physical or mental conditions that affect pain measurement after surgery
  • History of chronic use of analgesics such as NSAIDs or CNS depressants like antiepileptics
  • Bleeding disorders

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

Ain Shams University

Cairo, Egypt, 11591

Actively Recruiting

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Research Team

S

Sarah A Afifi, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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