Peri-operative antibiotics in tonsillectomy patients

Not Applicable

Completed

• Conditions: Pain; Surgery

• Registration Number: ISRCTN52345875
• Lead Sponsor: Department of Health (UK)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2003-09-12
• Study Completion: 2005-03-01
• Last Update Posted: 11 June 2018

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 186

Inclusion Criteria

Adult patients listed for tonsillectomy.

Exclusion Criteria

Does not meet inclusion criteria

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1. Visual analogue scale for pain at 24 h, 1 week, 2 weeks<br>2. Analgesia requirements at end of 2 weeks

Secondary Outcome Measures

Name	Time	Method
ot provided at time of registration