Comparison of Intrathecal 1% Chloroprocaine and 0.5% Hyperbaric Bupivacaine for Infraumbilical surgeries - A prospective randomized trial.
Not Applicable
- Conditions
- Health Condition 1: R688- Other general symptoms and signs
- Registration Number
- CTRI/2018/11/016249
- Lead Sponsor
- Department of Anaesthesia
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patient age between 18 - 60 years.
ASA physical Status 1 & 2
Exclusion Criteria
Age <18 & > 60 years
ASA physical status 3,4,5& 6
Patients refusal
Patient sensitive/ allergic to local anaesthetic agent.
Patient with peripheral sensorineural deficit
Patient on anticoagulants
Infection at the site of lumbar puncture
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Onset and duration of sensory blockTimepoint: 6 months
- Secondary Outcome Measures
Name Time Method Adverse effectsTimepoint: 6 months;Duration of analgesiaTimepoint: 6 months;Duration of motor blockTimepoint: 6 months;Hemodynamic effectsTimepoint: 6 months;Time to return of voiding function post-operatively.Timepoint: 6 months