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Comparison between two local anaesthetics for use in Spinal Anaesthesia in Patients undergoing Gynaecological Surgeries

Phase 4
Registration Number
CTRI/2023/09/057971
Lead Sponsor
Department of Anaesthesiology
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 elective gynaecological surgeries under spinal anaesthesia

2.patients who have given written informed consent to participate in the study

Exclusion Criteria

1. Patient with any contraindication to spinal anaesthesia

2. Patient having uncontrolled systemic disease

3. Patient undergoing emergency Surgery

4. Patient with known allergy to the drugs used

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
duration of sensory block produced after intrathecal administration <br/ ><br>Timepoint: Intraoperative and postoperative period
Secondary Outcome Measures
NameTimeMethod
compare the haemodynamic changes (heart rate, blood pressure) between the two groupsTimepoint: Intraoperative and postoperative period;compare the onset of motor (muscle paralysis) and sensory blocks with Ropivacaine vs Bupivacaine <br/ ><br>Timepoint: Intraoperative period;compare the time of first requirement of rescue analgesia (pain relief) in the patients of the two groupsTimepoint: Postoperative period
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