Pain Sensitivity and Outcome in Arthroscopic Shoulder Surgery

• Conditions: Anomaly; Shoulder

• Registration Number: NCT01621555
• Lead Sponsor: NHS Fife

Brief Summary

The purpose of this study is to investigate whether there is a correlation between a patients pain sensitivity and their subsequent post-operative pain and surgical outcome in arthroscopic shoulder surgery.

Detailed Description

Arthroscopic shoulder surgery is increasingly performed on a daycase basis. Optimal pain relief is the goal as this not only improves patient comfort and allows expedient discharge from hospital, but also reduces the risk of developing postoperative chronic pain and may improve surgical outcome. However, optimal postoperative pain control in daycase surgery remains a challenge. There is considerable variation in the level of postoperative pain experienced between individuals and subsequent analgesia requirements. Previous studies have attempted to predict the level of postoperative pain an individual will experience, using a variety of complex preoperative pain and psychological assessments. Other investigators have focused on a simpler approach, by testing an individual's pain threshold to a single preoperative nociceptive (painful) stimulus, e.g. heat or pressure. Recent work has produced a simple questionnaire alternative to pain intensity testing, the Pain Sensitivity Questionnaire (PSQ). We hypothesise that a patient's pain sensitivity preoperatively may both affect the level of pain they experience postoperatively and their final surgical outcome.

The aim of our study is to correlate a patient's pain sensitivity, as measured by the Pain Sensitivity Questionnaire, with the degree of acute postoperative pain (first 4 days) they experience and subsequent surgical outcome at 6 months.

Study Timeline

• Status Verified: 2012-06
• Study First Submitted: 2012-06-14
• Study First Submitted QC: 2012-06-14
• Last Update Submitted: 2012-06-14
• Study First Posted: 2012-06-18
• Last Update Posted: 2012-06-18
• Study Start: 2012-08
• Study Completion: 2014-11

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 200

Inclusion Criteria

All patients aged 18 years or older, attending for arthroscopic shoulder surgery (stabilisation, rotator cuff repair, arthrolysis, subacromial decompression), able to give informed consent.

Exclusion Criteria

• Unable to give informed consent
• Documented sensory abnormality (e.g. peripheral neuropathy)
• Contraindication to proposed anaesthetic/analgesic regimen
• No telephone or unable to communicate in English
• Documented psychiatric disorder
• Documented/suspected substance abuse

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Degree of correlation between Pain Sensitivity Questionnaire score and 6 month postoperative Rowe/Constant Score.	6 months

Secondary Outcome Measures

Name	Time	Method
The degree of correlation between Pain Sensitivity Questionnaire scores and 'Area Under the Curve (AUC)' for postoperative pain experienced (generated from the VAS scores over 4 postoperative days).	6 months
• The degree of correlation between AUC for postoperative pain and 6 month Constant/Rowe score.	6 months

Trial Locations

Locations (1)

NHS FIFE; 🇬🇧 Kirkcaldy, Fife, United Kingdom