comparison of 2 different doses of chlorprocaine in spinal anaesthesia for below umbilicus surgery
Not Applicable
Completed
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2019/12/022203
- Lead Sponsor
- K S Hegde medical Academy
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 32
Inclusion Criteria
Duration -Surgery <60minutes
BMI <35 kg/m2
elective surgery
surgeries below umbilicus
Exclusion Criteria
Emergency surgery
Pregnancy
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.To estimate and compare the time taken to reach maximal height of the block <br/ ><br> 2. To evaluate and compare duration of block <br/ ><br>Timepoint: 1.To estimate and compare the time taken to reach maximal height of the block <br/ ><br> 2. To evaluate and compare duration of block <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1.Hemodynamic parameter like heart rate and non invasive blood pressure <br/ ><br>2.Recovery from motor and sensory block (2 segment regression) <br/ ><br>3.Mobilisation without support <br/ ><br>4.First micturition <br/ ><br>5.Transient neurologic symptoms at 24hrs and at the end of 7 days. <br/ ><br> <br/ ><br>Timepoint: from starting of surgery till patient is shifted from postoperative care unit