To assess and compare the post-op analgesic effect of intrathecal Buprenorphine versus Fentanyl Citrate with control group, as an adjuvant to 0.5% hyperbaric Bupivacaine in lower abdominal surgeries.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/01/030624
- Lead Sponsor
- Sawai Man Singh Medical College And Attached Hospitals
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients Undergoing lower abdominal surgeries
Patients with Body Weight: 45 to 70 kg
Patients classified under American Society of Anesthesiologists as:
Grade I: Without Co- morbid Conditions
Grade II: Controlled Co- morbid Conditions
Exclusion Criteria
1. Patients not willing to participate in the study.
2. Cases with sepsis, bacteremia or skin infection of local site
3. History of severe hypovolemia, anemia and compromised renal,
cardiac or respiratory status
4. Cases with raised intracranial tension
5. History of blood coagulopathies
6. Patient allergic to drugs used for study
7. Uncooperative patients
8. Failure of spinal anesthesia, cases in which general anaesthesia will be required.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine the difference in mean time duration for the need of first rescue analgesia.Timepoint: 24 hours.
- Secondary Outcome Measures
Name Time Method 1.To assess and compare the onset time and duration of Sensory and Motor block. <br/ ><br>2.To assess and compare Hemodynamic parameters: (Heart Rate; Mean Blood Pressure; Systolic Blood Pressure; Diastolic Blood Pressure), Sedation score and VAS score. <br/ ><br>3.To find out and compare the proportion of cases with complications. <br/ ><br>Timepoint: 24 hours.