Comparison of two local anesthetics for spinal anesthesia in caesarean sectio
Not Applicable
- Conditions
- Health Condition 1: O94- Sequelae of complication of pregnancy, childbirth, and the puerperium
- Registration Number
- CTRI/2024/01/061890
- Lead Sponsor
- Dr Shivakumar G
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients posted for elective caesarean section surgeries.
Age group 18 to 40 years.
Patients with height 150cm-180cm and weight 40kg-80kg.
Patients with American Society of Anaesthesiologists-Physical status (ASA-PS) grade I and II.
Patients willing to give informed consent to participate in the study.
Exclusion Criteria
Patients with cardiovascular diseases or pregnancy induced hypertension and gestational diabetes mellitus.
Patients having increased intracranial tension, severe hypovolemia, history of bleeding diathesis and local infection.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method