Effect of Pregabalin on Shoulder Pain in Patients With Central Sensitization After Arthroscopic Rotator Cuff Repair

Phase 4

Not yet recruiting

• Conditions: Rotator Cuff Tears; Central Sensitisation; Neuropathic Pain

• Registration Number: NCT06367998
• Lead Sponsor: The Catholic University of Korea

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-4-11
• Last Update Posted: 2 September 2024

Recruitment & Eligibility

• Status: Not yet recruiting
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

Inclusion Criteria:<br><br> - Age over 19 to under 70<br><br> - Underwent arthroscopic rotator cuff repair due to a tear of the rotator cuff.<br><br> - Clinical diagnosis of myofascial pain syndrome<br><br> - Central sensitization (Central Sensitization Inventory (CSI) score of 40 or above).<br><br>Exclusion Criteria:<br><br> - Previous history of Pregabalin prescription<br><br> - Hypersensitivity reactions or severe complications after taking Pregabalin.<br><br> - Diagnosed with and are being treated for psychiatric disorders<br><br> - Localized infection, sepsis, or previous neurological abnormalities<br><br> - Uncontrolled hypertension (evidenced by a resting blood pressure of more than 100<br> mmHg)<br><br> - Liver function abnormalities (aspartate aminotransferase or alanine aminotransferase<br> >60 IU/litre).<br><br> - major cardiovascular diseases or renal impairments

Exclusion Criteria

Not provided

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The Visual Analogue Scale (VAS) pain score

Secondary Outcome Measures

Name	Time	Method
Constant shoulder score;American shouler and elbow surgeons (ASES) score