MedPath

Antibiotic used in Inguinal Hernia repair

Phase 1
Conditions
Health Condition 1: K402- Bilateral inguinal hernia, withoutobstruction or gangrene
Registration Number
CTRI/2021/12/038794
Lead Sponsor
Dr Samit Doshi
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1) All patients undergoing elective open inguinal mesh hernioplasty.

2) Patients with Unilateral inguinal hernia and Bilateral inguinal hernia.

3) Patients giving consent for taking part in the study.

4) Patients above 18 years of age.

5) All clean hernia surgeries.

Exclusion Criteria

1) Patients below 18 years of age.

2) All the other hernias except inguinal hernias.

3) Patients on steroid treatment or patients with immunosuppressed states and malignancy.

4) Patients having local site infections like Tinea or Scabies.

5) All patients with complicated hernia such as Irreducible hernia, Obstructed hernia and Strangulated hernia. 6) All patients allergic to Cephalosporins.

7) All Laparoscopic hernia repairs.

8) All Recurrent inguinal hernias.

9) All clean-contaminated, contaminated and dirty hernia surgeries.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
From this study it is expected that <br/ ><br>1) multiple dose Cefotaxime does not cause a significant decrease in the rate of surgical site infection compared to single dose Cefotaxime <br/ ><br>2) Lower treatment costs for the patient and is cost effective <br/ ><br>3) Reduce the spread of antibiotic resistance <br/ ><br>4) Avoidance of side effects due to overuse of antibiotics <br/ ><br>5) Reduce hospital stayTimepoint: Assessment of patients to evaluate surgical site infection on day 3 day 5 day 7 day 15 and day 30
Secondary Outcome Measures
NameTimeMethod
noneTimepoint: none
© Copyright 2025. All Rights Reserved by MedPath