A RESEARCH ABOUT THE PAIN RELIEVING EFFECT OF THE MEDICINE, GABAPENTIN, WHEN GIVEN BEFORE SURGERY, IN THE CASE OF UTERUS REMOVAL OPERATION DONE UNDER SPINAL ANAESTHESIA
Not Applicable
- Conditions
- Health Condition 1: null- Female Patients undergoing Total Abdominal Hysterectomy
- Registration Number
- CTRI/2014/06/004674
- Lead Sponsor
- Robert James Premkumar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
ASA Grade I and II undergoing Total Abdominal Hysterectomy
Exclusion Criteria
Denial of consent, Allergy to Gabapentin, Consumption of NSAID in last 48 hrs, Patients Suffering from epilepsy, liver disease, renal disease, chronic pain syndrome, Patients who have psychiatric illness
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method VISUAL ANALOGUE SCALE Pain ScoreTimepoint: 2, 4, 8, 12, 24 Hours after surgery
- Secondary Outcome Measures
Name Time Method The amount of rescue analgesic consumptionTimepoint: 0-2, 2-4, 4-8, 8-12, 12-24 Hours after Surgery