To compare two spinal anaesthetic drug with additive for lower abdominal surgeries

Phase 4

• Conditions: Health Condition 1: M238- Other internal derangements of knee

• Registration Number: CTRI/2024/08/071933
• Lead Sponsor: Dr Anul R Shinde

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

Age 18-60 years

Either gender

American Society of Anesthesiologists (ASA) grade I and II patients

Patients undergoing infraumbilical surgeries under spinal anesthesia

Exclusion Criteria

Patients with American Society of Anesthesiologists (ASA) grade III or more

Patients with allergy to study drug

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To study the effect of intrathecal buprenorphine as an adjuvant to 0.5% hyperbaric bupivacaine and 0.5% hyperbaric levobupivacaine on hemodynamic parameters (HR, SBP, DBP, MAP, SpO2 ) in adults undergoing infraumbilical surgeries under spinal anesthesia.Timepoint: Pre operative, 0 minute, 5 minutes, 15 minutes

Secondary Outcome Measures

Name	Time	Method
- To evaluate and compare the onset of sensory and motor blockade of intrathecal buprenorphine as an adjuvant to 0.5% hyperbaric bupivacaine and 0.5% hyperbaric levobupivacaine in adults undergoing infraumbilical surgeries under spinal anesthesia.Timepoint: 0 minute <br/ ><br>1 minute <br/ ><br>2 minutes <br/ ><br>3 minutes <br/ ><br>4 minutes <br/ ><br>5 minutes