To Compare the effects two different Opiods in spinal anaesthesia for Infraumbilical surgeries
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/08/056068
- Lead Sponsor
- Goa medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Weight:50-60kgs
Age:18-60yrs
Of either sex
ASA grade 1 and 2
Exclusion Criteria
Patients declining consent
Patients with local infection
Patients with raised intracranial pressure
Pregnant and lactating females
Coagulopathies
Patients allergic to local anaesthetic
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Maximum sensory block height reached time taken to regress to T12 dermatome time taken for complete motor recovery and heart rate blood pressure respiratory rate and spo2 will be monitoredTimepoint: Maximum sensory block height reached time taken to regress to T12 dermatome time taken for complete motor recovery and heart rate blood pressure respiratory rate and spo2 will be monitored at 5,10,15,30min and so on till 24 hrs
- Secondary Outcome Measures
Name Time Method Duration of analgesia and complications associated can be studiedTimepoint: 5min <br/ ><br>Till <br/ ><br>120min