Comparison between hyperbaric Ropivacaine and hyperbaric Bupivacaine in patients undergoing inguinal and perineal surgeries under spinal anaesthesia.
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/02/050035
- Lead Sponsor
- Dr D Y Patil Medical college Hospital and Research Centre Pune
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1. Patients undergoing inguinal and perineal surgeries under spinal anesthesia.
2. Hemodynamically stable patients with all routine investigations within normal limits with no co-morbidities.
3. Patients who are not on any cardiac related drugs.
4. Availability of informed consent.
1. Patients with ASA physical status 3 or more.
2. Patients below 18 years and above 60 years of age.
3. Patients posted for emergency procedures.
4. Patients with major neurological, cardiac, respiratory, metabolic, renal, hepatic
disease or any coagulation abnormalities.
5. Patients contraindicated for spinal anesthesia.
6. Patients with known allergies to the study drugs.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time taken for the onset of sensory block followed by <br/ ><br>Time taken to T8 level sensory blockade post subarachnoid block with either injection bupivacaine heavy or injection ropivacaine heavy. <br/ ><br>Timepoint: 2 minutes to 15 minutes
- Secondary Outcome Measures
Name Time Method 5.To observe for any incidence of adverse events and for the need of general anesthesia (GA) supplementation.Timepoint: 2 to 20 minutes;Duration of sensory blockadeTimepoint: 150 minutes;Intraoperative hemodynamic parameters like heart rate, blood pressureTimepoint: 2 minutes to 150 minutes;Onset and duration of motor blockadeTimepoint: 2 minutes to 150 minutes;Time of first micuritionTimepoint: At 120 to 150 minutes post subarachnoid block