Comparison of chloroprocaine and bupivacaine for SUBARACHNOID BLOCK
Not Applicable
Completed
- Conditions
- Health Condition 1: O269- Pregnancy related conditions, unspecified
- Registration Number
- CTRI/2021/02/031464
- Lead Sponsor
- Dr SUJEET RAI
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 96
Inclusion Criteria
Pregnant Female patients aged between 18-35 years undergoing elective caesarean section of American society of anaesthesiology (ASA) physical status I and II and giving consent will be included.
Exclusion Criteria
Patient refusal or uncooperative patients, Patients with severe cardiopulmonary disease, allergy or intolerance to local anaesthetics, coagulation disorders, neurologic disease or spine deformities, Infection at the site of needle insertion, of ASA physical status 3 and 4 will be excluded.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate and compare the efficacy of Chloroprocaine HCI 1 percent with Hyperbaric Bupivacaine 0.5 percent in spinal anaesthesia for lower segment caesarean section on the basis of duration of analgesia peak height of block time of onset recovery and time of ambulationTimepoint: 1 year
- Secondary Outcome Measures
Name Time Method To evaluate and compare the efficacy of Chloroprocaine HCI 1 percent with Hyperbaric Bupivacaine 0.5 percent in spinal anaesthesia for lower segment caesarean section on the basis of duration of analgesia peak height of block time of onset recovery and time of ambulationTimepoint: 1 year