A study to compare the clinical features of drugs 0.75% ropivacaine and the combination of ropivacaine 0.75% with fentanyl 25 mcg for spinal anaesthesia in patients undergoing perianal surgeries
Phase 1
- Conditions
- Health Condition 1: 8- Other Procedures
- Registration Number
- CTRI/2024/02/063007
- Lead Sponsor
- Dr ARUNKUMAR A BARASAKALE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
a) Patients aged between 18 to 60 years of age posted for elective perianal
surgeries.
b) ASA grade I and II patient
Exclusion Criteria
a)Patients who has H/o coagulation and bleeding disorders.
b) Local site infections.
c) H/o hypersensitivity to study drugs.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.Time taken for ambulation without assistance.Timepoint: 24 hours
- Secondary Outcome Measures
Name Time Method 1.Time to achieve T10 sensory block <br/ ><br>2.Maximum height of sensory block <br/ ><br>3.Duration of sensory block <br/ ><br>4.Duration of motor blockTimepoint: 24 HOURS