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Comparison of Post Operative Analgesic Properties of Intrathecal Buprenorphine Versus Magnesium Sulphate as Adjuvants to 0.5% Hyperbaric Bupivacaine for Lower Abdominal Surgeries

Not Applicable
Conditions
Health Condition 1: N80-N98- Noninflammatory disorders of female genital tract
Registration Number
CTRI/2020/06/025962
Lead Sponsor
Department of Anesthesiology
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
NameTimeMethod
To assess and compare the duration of analgesiaTimepoint: 24 hours
Secondary Outcome Measures
NameTimeMethod
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
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