Duration of Pain relief using two different intrathecal opoids (Nalbuphine vs. Fentanyl) in lower limb surgeries.
Not Applicable
- Conditions
- Health Condition 1: null- Age between 18 to 60 years, ASA I and II, both male and female patients undergoing lower limb surgery.
- Registration Number
- CTRI/2017/05/008588
- Lead Sponsor
- one
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
Patients aged between 18 to 60 yrs with ASA I & II, of either sex, undergoing lower limb surgeries.
Exclusion Criteria
-Pre-existing neurological deficit/peripheral neuropathy
-Coagulation disorders
-Local infection at the site of block.
-Pregnancy
-History of allergy to amide local anesthetics
-Patient refusal to participate in the study
-Patient having cardio or respiratory system failure
-Uncooperative patients.
-Patient with h/o end organ damage
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of Analgesia and block characteristicsTimepoint: 12 hr.
- Secondary Outcome Measures
Name Time Method Hemodynamics and adverse eventTimepoint: 12 hr.