Effect of Dexmedetomidine- Fentanil on postoperative pain of spine surgery
Phase 3
- Conditions
- spinal surgery.
- Registration Number
- IRCT20110402006115N4
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 66
Inclusion Criteria
The candidate for the posterior fusion of the lower back and the thoracic spine
Age range 20 to 70 years
Patients ASA 1 or 2
Satisfaction to participate in the study
Educable and have the ability to cooperate
Exclusion Criteria
History of acute allergic reaction to Dexmedetomidine or Fentanil
Patients with mental and physical disabilities in the application of pain pumps
The presence of any moderate to severe CVD and respiratory instability
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain score base on VAS criteria. Timepoint: Start logging in to recovery, every hour to 24 hours. Method of measurement: VAS CRITERIA SCORE.
- Secondary Outcome Measures
Name Time Method