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Comparison between hyperbaric Ropivacaine and hyperbaric Bupivacaine in patients undergoing inguinal and perineal surgeries under spinal anaesthesia.

Not Applicable
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
Inclusion Criteria

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.

Exclusion Criteria

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
NameTimeMethod
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
NameTimeMethod
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
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