COMPARISON BETWEEN TWO DIFFERENT DOSES (300MG AND 600MG) OF THE DRUG GABAPENTIN TO ASSESS POST OPERATIVE PAIN TOLERANCE OF PATIENTS UNDERGEOING LOWER LIMB SURGERIES UNDER SPINAL ANAESTHESIA
Phase 4
- Registration Number
- CTRI/2019/01/017145
- Lead Sponsor
- MGM MEDICAL COLLEGE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
BOTH MALE AND FEMALE PATIENTS OF AGE GROUP 18-65 YRS RECEIVING SPINAL ANAESTHESIA FOR ELECTIVE LOWER LIMB SURGERIES UNDER ASA GRADE 1 AND 2
Exclusion Criteria
1. PATIENTS WITH ALLERGY TO GABAPENTIN
2. PATIENTS SUFFERING FROM EPILEPSY, LIVER AND RENAL DISEASE, ANY CHRONIC PAIN SYNDROMES, PSYCHIATRIC ILLNESS
3. PATIENTS REQUIRING SURGICAL DURATION MORE THAN 3 HOURS
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method COMPARE TOTAL DURATION OF ANALGESIA AND TOTAL NUMBER OF ANALGESICS REQUIRED IN THE FIRST 24 HOURS AFTER SURGERYTimepoint: 24 HOURS
- Secondary Outcome Measures
Name Time Method COMPARE SIDE EFFECTS OF THE TWO DOSES OF GABAPENTIN IF ANYTimepoint: 24 HOURS