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NOT YET RECRUITING
NCT06367998
PHASE4

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

Sponsor: The Catholic University of Korea

View on ClinicalTrials.gov

Summary

This study aims to investigate the effects of Pregabalin intake on shoulder pain management in patients with central sensitization undergoing arthroscopic rotator cuff repair. Although Pregabalin is known to be effective in controlling pain after shoulder arthroscopy, research on its efficacy in pain management for patients with central sensitization is scarce. Utilizing a list that identifies central sensitization, this study will explore whether Pregabalin can reduce postoperative pain in these patients and potentially improve joint mobility, emotional, and physical functioning. A prospective randomized study is planned, with inclusion criteria set for patients aged between 19 and 70 who have undergone arthroscopic rotator cuff repair. The study will compare clinical outcomes up to one year postoperatively between two groups of 38 patients each. The case group will receive standard postoperative medications (NSAIDs) plus Pregabalin oral intake from the day before surgery to six weeks postoperatively, while the control group will receive only the standard postoperative medications without Pregabalin.

Official title: The Effect of Pregabalin on Shoulder Pain of Patients With Myofascial Pain Syndrome and Central Sensitization Who Undergo Arthroscopic Rotator Cuff Repair

Key Details

Gender

All

Age Range

20 Years - 69 Years

Study Type

INTERVENTIONAL

Enrollment

76

Start Date

2024-09-01

Completion Date

2026-05-01

Last Updated

2024-08-23

Healthy Volunteers

Yes

Interventions

DRUG

Pregabalin

Pregabalin oral intake from the day before surgery to six weeks postoperatively