A clinical study to evaluate effectiveness of drug tramadol for pain free period after gynecological surgeries
Not Applicable
- Conditions
- Health Condition 1: N80-N98- Noninflammatory disorders of female genital tract
- Registration Number
- CTRI/2020/08/027221
- Lead Sponsor
- Shree krishna hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA grade 1-3 physical status
Exclusion Criteria
Hypersensitivity to local anesthetics, absolute contraindications to spinal anesthesia that is patients refusal, any bleeding diathesis patients, local site infection,relative contraindications like severe hypotension, obstructive cardiomyopathies, any spinal deformity, spinal cord injnury
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Parameter that will be used to evaluate effect of addition of tramadol in post-operative analgesic effect of drug is VISUAL ANALOG SCALE (VAS) SCORE. VAS score will be assessed every 40 minute interval till 6 hours post-operatively for the first analgesic requirement.Timepoint: Parameter that will be used to evaluate effect of addition of tramadol in post-operative analgesic effect of drug is VISUAL ANALOG SCALE (VAS) SCORE. VAS score will be assessed every 40 minute interval till 6 hours post-operatively for the first analgesic requirement.
- Secondary Outcome Measures
Name Time Method Hemodynamic stability. PARAMETERS that will be assessed are HYPOTENSION, BRADYCARDIA, ARRYTHMIAS, DESATURATION and side effects like NAUSEA, VOMITTING, PRURITUS, SHIVERING and URINARY RETENTION in patients undergoing gynecological surgeries. THIS PARAMETERS WILL BE ASSESSED INTRA-OPERATIVELY THROUGHT THE SURGERY.Timepoint: Hemodynamic stability. PARAMETERS that will be assessed are HYPOTENSION, BRADYCARDIA, ARRYTHMIAS, DESATURATION and side effects like NAUSEA, VOMITTING, PRURITUS, SHIVERING and URINARY RETENTION in patients undergoing gynecological surgeries. THIS PARAMETERS WILL BE ASSESSED INTRA-OPERATIVELY THROUGHT THE SURGERY.