Transdermal lidocaine patch for acute postoperative pain in laparoscopic gynecologic operation: A randomized controlled trial

Phase 4

Recruiting

• Conditions: non-malignancy gynecologic condition; Transdermal lidocaine patch; acute postoperative pain; laparoscopic gynecologic operation

• Registration Number: TCTR20210707001
• Lead Sponsor: /A

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-07-07
• Study Completion: 2021-08-11
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 110

Inclusion Criteria

Age 18-65 years old
Laparoscopic gynecologic procedure

Exclusion Criteria

Opioid allergy

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
dose of morphine use comparing between 2 group 6 , 12 , 24 hr milligram

Secondary Outcome Measures

Name	Time	Method
Postoperative pain score 6 , 12 , 24 hr point,Postoperative nausea and vomiting 6 , 12 , 24 hr times,Skin reactions at the application site 6 , 12 , 24 hr yes or no