The effect of pain control pump for postoperative cuff repair

Phase 2

• Conditions: Rupture of rotator cuff tendon.; Rotator cuff tear or rupture, not specified as traumatic; M75.1

• Registration Number: IRCT20091117002723N3
• Lead Sponsor: Shiraz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 70

Inclusion Criteria

Adult patients with ASA grade I or II (American Society of Anesthesiology classification)
patients between 30 and 70 years old
Patients who candidate for rotator cuff surgery

Exclusion Criteria

Allergy to the drugs used in the study
Positive history of chemotherapy and radiotherapy
Positive history of liver, kidney, hormone problems, central nervous system disorders and diseases, depression and anxiety
Addiction to drugs, alcohol and smoking
Use of Corticosteroid and Benzodiazepine
pregnancy

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Every 10 minutes during recovery, 6 hours, 12 hours, 24 hours, 48 hours, one week, ten days and two weeks after the end of the intervention. Method of measurement: Questionnaire and Numerical Pain Rating Scale (NRS).