Survey of the effect of gabapentin on post-operative pain of shoulder rotator cuff surgery
Phase 2
Recruiting
- Conditions
- Shoulder rotator cuff surgery.Rotator cuff tear or rupture, not specified as traumaticM75.1
- Registration Number
- IRCT20100127003213N9
- Lead Sponsor
- Shiraz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Patients undergoing shoulder rotator cuff surgery
Age 30-65 years old
(ASA) I-II
Exclusion Criteria
Sensitivity to gabapentin
History of hypertension
Heart disease
Liver and kidney disease
Acute or chronic pain associated with other areas of the body
Any dependence on narcotics and psychotropic drugs
Continuous use of tranquilizers for depression and anxiety disorders and seizure disorders
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: The severity of pain is measured by Numeric Rating Scale , every 2 hours to 6 hours, and then every 6 hours to 24 hours. Method of measurement: Numeric Rating Scale (NRS).
- Secondary Outcome Measures
Name Time Method