The rationale of study is that which one among Nalbuphine and Buprenorphine,is a better adjuvant yet to be explored as only few studies happened in past on this
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/03/050389
- Lead Sponsor
- ROHILKHAND MEDICAL COLLEGE AND HOSPITA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
American society of Anesthesiologists (ASA) grade 1 or 2
Posted for surgeries of lower abdomen or lower limb of different surgical specialities
Exclusion Criteria
Patient refusal for procedure
Any Neuropathy,Cardiac disease,diabetes,Nephropathy,Coagulopathy
Any known allergy to local anaesthetic
Patients with contraindications for spinal anaesthesia such as derranged coagulation profile ,raised ICP,local infection at site of needle insertion
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Onset of sensory and motor block <br/ ><br>Duration of sensory and motor block <br/ ><br>Duration of postoperative analgesia <br/ ><br> <br/ ><br>Timepoint: At 2,4,6,8,10,12,14,16,18,20,30,40,50,60,90,120,180,240,360,720 minutes after block , heart rate ,ECG lead 2 ,systolic , diastolic and mean blood pressure and oxygen saturation will be recorded <br/ ><br> <br/ ><br>
- Secondary Outcome Measures
Name Time Method Hemodynamic responses to the drug during and after surgery <br/ ><br>Any complication or side effectsTimepoint: At 2,4,6,8,10,12,14,16,18,20,30,40,50,60.90,120,180,240,360,480,720 minutes after the block , heart rate ,ECG lead 2,systolic,diastolic and mean blood pressure and oxygen saturation will be recorded