Comparison of two drugs in spinal anesthesia for pain relief in post operative period
Phase 2
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/03/031729
- Lead Sponsor
- Pims
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1Patients belonging to ASA I & II
2Aged between 18 & 65 years
3 Patient undergoing elective infra umbilical surgeries
Exclusion Criteria
1Patients with raised intracranial pressure or any intracranial pathology
2 Hypovolemia, Bradycardia
3 Patients on anticoagulants
4 Localised infection
5 Pregnant women
6 Allergy to local anaesthetics.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method to compare the duration of analgesia of nalbuphine and fentanyl in postoperative period in addition to bupivacaine in spinal anesthesia by using VAS scoreTimepoint: 24 hours
- Secondary Outcome Measures
Name Time Method 1) to compare the onset and duration of sensory and motor blockade <br/ ><br>2)to compare the hemodynamic parametersTimepoint: 24hours