A clinical study comparing two different types of Spinal anaesthesia in patients undergoing elective urological endoscopic surgeries
Phase 2
Completed
- Conditions
- Health Condition 1: N401- Benign prostatic hyperplasia withlower urinary tract symptomsHealth Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2024/03/063770
- Lead Sponsor
- Institute of Medical Sciences and SUM Hospital Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 76
Inclusion Criteria
1. Patients undergoing elective urological surgeries
2. Patients within the age group of 18 to 60 years
3. Patients under ASA 1 and 2.
Exclusion Criteria
1. Patient who are not willing to give consent for the study.
2. Patient known allergic to local anesthetic agents
3. Neurological, cardiovascular, respiratory, renal diseases
4. Platelet and coagulation disorders
5. Spine deformities or skin infection at local sites.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intraoperative quality of anaesthesia (scores given from 1-4) <br/ ><br>Timepoint: 0and 1hour
- Secondary Outcome Measures
Name Time Method to determine onset & duration of sensory blockade & motor blockade, incidence of hypotension & bradycardia & time taken to walk unaided. <br/ ><br>Timepoint: Onset of sensory block <br/ ><br>at the level of T10, <br/ ><br>Onset of motor block modified Bromage score 2, <br/ ><br>Duration of sensory block till regression to L1, <br/ ><br>Duration of motor block till recovery to Bromage score 6 <br/ ><br>