albuphine and Fentanyl a comparative study in infraumbilical surgeries
Not Applicable
Completed
- Conditions
- Health Condition 1: N938- Other specified abnormal uterine and vaginal bleeding
- Registration Number
- CTRI/2019/01/016945
- Lead Sponsor
- MOSC medical CollegeKolenchery
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 70
Inclusion Criteria
1.Age 20-60 years of either gender.
2.American Society of Anaesthesiologists (ASA) grade 1 and 2 patients.
3.Patients undergoing elective infraumbilical surgeries like abdominal hysterectomy, open inguinal hernia repair under spinal anesthesia
Exclusion Criteria
1.known hypersensitivity to any of the study drugs.
2.Contraindications to central neuraxial block
3.Pregnancy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1) To compare the duration of analgesia between Nalbuphine and Fentanyl as adjuvants to intrathecal hyperbaric 0.5% Bupivacaine in patients undergoing infraumbilical surgeriesTimepoint: Verbal numerical pain rating scale score(Verbal NPRS score) <br/ ><br>Before spinal <br/ ><br>At incision <br/ ><br>Post incision <br/ ><br>min 30 <br/ ><br>min 60 <br/ ><br>min 90 <br/ ><br>min 120 <br/ ><br>min 150 <br/ ><br>min 180 <br/ ><br>PACU(Hourly):4th,5th,6th,7th <br/ ><br>8th hr <br/ ><br>12th hr <br/ ><br>16th hr <br/ ><br> <br/ ><br>
- Secondary Outcome Measures
Name Time Method