comparison of drug and placebo for post operative pain relief in patients undergoing uterus removal surgery under spinal anaesthesia
Not Applicable
- Conditions
- Health Condition 1: N92- Excessive, frequent and irregularmenstruationHealth Condition 2: D25- Leiomyoma of uterusHealth Condition 3: O- Medical and SurgicalHealth Condition 4: N93- Other abnormal uterine and vaginalbleeding
- Registration Number
- CTRI/2021/08/035563
- Lead Sponsor
- GOVERNMENT MEDICAL COLLEGE BHAVNAGAR
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patients undergoing elective abdominal hysterectomy
2. Patients with ASA Grade I/II
Exclusion Criteria
1. Patient in whom spinal anaesthesia is contraindicated (i.e. Altered coagulation profile, Any spinal deformity)
2. Patients in whom Gabapentin is contraindicated (i.e. allergic to gabapentin and Patients with history of vertigo, liver & kidney disease)
3. Chronic pain syndromes
4. Patients with recent analgesic use
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method