Status:

COMPLETED

The Effect of Postoperative Modified Trendelenburg Position to Decrease Shoulder Pain After Laparoscopic Hysterectomy: A Randomized Controlled Trial

Lead Sponsor:

Department of Medical Services Ministry of Public Health of Thailand

Conditions:

Post Operative Pain

Shoulder Pain

Eligibility:

FEMALE

30-65 years

Phase:

NA

Brief Summary

Laparoscopic surgery is commonly used procedure in diagnostic and treatment including Hysterectomy. Post laparoscopic shoulder pain is common side effect mostly occur after surgery. Postoperative Tren...

Detailed Description

After laparoscopic hysterectomy surgery, Patients in intervention group were positioned in a Modified Trendelenburg position (20 °) postoperative for 6 hours because of the limitation of this study ca...

Eligibility Criteria

Inclusion

  • Female patient age between 30-65 years
  • American Society of Anesthesiologist (ASA) physical status I or II
  • Scheduled for operative laparoscopic hysterectomy with abdominal incisions measuring less than 1 cm in size
  • Can speak and understand Thai language

Exclusion

  • Pregnant women
  • Conversion procedure to open abdominal surgery
  • Patients with postoperative abdominal drainage
  • Surgery duration more than 3 hours
  • Gynecologic malignancy surgery
  • Patients with history of chronic shoulder pain
  • Patients with history of previous shoulder surgery
  • Inability to accurately express pain
  • Patients with history of Gastroesophageal reflux disease or chronic gastritis
  • Patients with history of cardiovascular or pulmonary disease
  • Patients with history of venous thrombosis
  • Morbid obesity BMI \> 40 kg/m2
  • Patients with history of increase intracranial pressure
  • Patients with history of increase intraocular pressure
  • Patients with liver and/or kidney disease
  • NSAIDs and/or Paracetamol and/or Morphine allergy
  • Current corticosteroid use
  • Patients who use current analgesic drugs and don't want to quit while stay in the hospital
  • Psychiatric disorder
  • Intellectual disorder
  • Postoperative length in hospital less than 24 hours

Key Trial Info

Start Date :

June 30 2022

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

August 30 2023

Estimated Enrollment :

46 Patients enrolled

Trial Details

Trial ID

NCT05428982

Start Date

June 30 2022

End Date

August 30 2023

Last Update

November 18 2023

Active Locations (1)

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1

Rajavithi Hospital

Bangkok, Thailand, 10400