comparison of two drugs given in spine area in patients posted for surgery in lower abdomen and lower limbs
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/05/052154
- 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
American society of anaesthesiology grade I and II patients scheduled for elective infraumbilical surgeries under spinal anaesthesia
Exclusion Criteria
1. patients with known allergy to any of the study drugs
2. patients with coagulation disorders and on anticoagulants
3. patients with local skin infection or disease
4. patients with previous spine surgery or spine abnormality
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method onset and duration of sensory blockTimepoint: from time of injection of drug till loss of sensation at T6 dermatome which will be checked every 2 minutes till 20 min and then every 10 min till highest level attained
- Secondary Outcome Measures
Name Time Method onset and duration of motor blockTimepoint: every 5 minutes for 30 minutes and then every 15 minutes till recovery of motor blockade to modified bromage score of zero