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Comparison of Efficacy of Two Different Techniques for Postoperative Pain Relief

Phase 2
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2023/01/049087
Lead Sponsor
SAPTHGIRI INSTITUTE OF MEDICAL SCIENCE AND RESEARCH CENTRE
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

ASA 1 AND 2 PHYSICAL STATUS

Exclusion Criteria

PATIENT NOT WILLING TO GIVE CONSENT FOR THE STUDY

BMI >35KG/M2

ALLERGIES/CONTRAINDICATIONS TO ANY OF THE DRUGS USED IN THE STUDY

PATIENTS ON PREOPERATIVE OPIOD OR NON STEROIDAL ANTI-INFLAMMATORY DRUG TREATMENTS FOR CHRONIC PAI

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
DURATION OF POST OPERATIVE ANALGESIA IN BOTH THE TECHNIQUES FOR 24 HRSTimepoint: DURATION OF POST OPERATIVE ANALGESIA IN BOTH THE TECHNIQUES FOR 24 HRS
Secondary Outcome Measures
NameTimeMethod
TO EVALUATE THE TIME TAKEN FOR ADMINISTRATION OF FIRST RESCUE ANALGESIATimepoint: FROM THE TIME OF DRUG INJECTION TILL 24 HOURS
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