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Comparing two different ultrasound guided nerve block for post operative pain relief in inguinal hernia surgeries

Not Applicable
Conditions
Health Condition 1: K409- Unilateral inguinal hernia, without obstruction or gangrene
Registration Number
CTRI/2020/07/026566
Lead Sponsor
S N Medical college and HSK hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1. ASA I-II Patients.

2. Patients undergoing elective unilateral inguinal

hernia repair.

Exclusion Criteria

1. Refusal at enrolment.

2. Patients with coagulation system disorders.

3. Patients with raised intra cranial tension.

4. Patients with fixed cardiac output states.

5. Patients with hepatic or renal failure.

6. Chronic use of opioids or corticosteroids.

7. Patients allergic to the drugs/ Local

anaesthetics to be used for the study

8. Infection at injection site

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Duration of post operative analgesia will be assessed after giving ultrasound guided blockTimepoint: 24 hours after the block
Secondary Outcome Measures
NameTimeMethod
oneTimepoint: not applicable
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