A randomized, placebo controlled, trial of preoperative sustained release betamethasone plus non-controlled intraoperative ketorolac or fentanyl on pain after diagnostic laparoscopy or laparoscopic tubal ligatio

Completed

• Conditions: Postoperative pain; Signs and Symptoms; Pain

• Registration Number: ISRCTN52633712
• Lead Sponsor: niversity of Tennessee Anesthesiology Research Fund (USA)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2003-08-19
• Last Update Posted: 13 January 2015

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 74

Inclusion Criteria

Patients undergoing laparoscopic surgery at University of Tennessee Medical Centre
Knoxville, Tennessee (USA)

Exclusion Criteria

Not provided at time of registration

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
ot provided at time of registration

Secondary Outcome Measures

Name	Time	Method
ot provided at time of registration