Evaluation of Postoperative Pain Following Bascom Cleft Lift Operation

Completed

• Conditions: Postoperative Pain

• Registration Number: NCT02196727
• Lead Sponsor: Hvidovre University Hospital

Brief Summary

The purpose of this study is to evaluate postoperative pain in Bascom Cleft Lift operation receiving multimodal analgesia in day-case surgery setting.

Hypothesis: Multimodal analgesia provides adequate pain relief in patients undergoing Bascom Cleft Lift operation.

Detailed Description

Not available

Study Timeline

• Status Verified: 2013-05
• Study Start: 2013-05
• Primary Completion: 2014-01
• Study Completion: 2014-04
• Study First Submitted: 2014-07-18
• Study First Submitted QC: 2014-07-21
• Last Update Submitted: 2014-07-21
• Study First Posted: 2014-07-22
• Last Update Posted: 2014-07-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 32

Inclusion Criteria

• Age > 18
• ASA physical status 1 and 2
• Patient undergoing Bascom operation in prone position

Exclusion Criteria

• Pregnancy
• Current regular use of drug belonging to the class of opioids
• Allergy/ intolerance to drugs included in multimodal analgesia regime

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Numerical Rating Scale (NRS) pain score (0=no pain, 10= maximum imaginable pain)	24 hours postoperatively

Secondary Outcome Measures

Name	Time	Method
Numerical Rating Scale (NRS) pain score (0=no pain, 10= maximum imaginable pain)	2 hours, 48 hours and 30 days postoperatively

Trial Locations

Locations (1)

Hvidovre Univarsity Hospital; 🇩🇰 Hvidovre, Copenhagen, Denmark