Effect Of Preemptive Gabapentin On Postoperative Pain Management After VATS Surgery
Phase 3
Recruiting
- Conditions
- Respiratory disease.Chronic lower respiratory diseases,Diseases of the respiratory system,Other diseases of upper respiratory tract,Other diseases of pleuraJ40-J47,J0
- Registration Number
- IRCT20160813029327N12
- Lead Sponsor
- Islamic Azad University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
between 18 and 65 years
proper physical condition for VATS surgery
Exclusion Criteria
gabapentin allergy
renal failure
hepatic failure
nervous and mental disorders
history of cardiovascular surgeries
pregnant and breastfeeding women
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain assessment. Timepoint: each 30 minutes and then 2, 4, 6, 10 and 24 hours after operation. Method of measurement: VAS technique.;Opioid rate of consumption. Timepoint: up to 24 hours after operation. Method of measurement: Based on nursing chart.;Ketorolac rate of consumption. Timepoint: up to 24 hours after operation. Method of measurement: Based on nursing chart.;First analgesic need time. Timepoint: first analgesic need time after surgery. Method of measurement: Based on nursing chart.
- Secondary Outcome Measures
Name Time Method Adverse reactions. Timepoint: up to 24 hours after operation. Method of measurement: questionnaire.