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se of Peroperative Antibiotics in Patients Undergoing Surgery For Breast Cancer

Not Applicable
Completed
Conditions
Health Condition 1: null- Patients with proven diagnosis of carcinoma breast planned for modified radical mastectomy as decided by institute tumor board
Registration Number
CTRI/2017/02/007790
Lead Sponsor
JIPMER
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
200
Inclusion Criteria

PATIENTS WHO ARE DIAGNOSED CASES OF CARCINOMA BREAST WHO ARE PLANNED TO UNDERGO MODIFIED RADICAL MASTECTOMY AS DECIDED BY THE INSTITUTE TUMOR BOARD

Exclusion Criteria

Exclusion criteria

1. Hypersensitivity to intravenous Cefazolin

2.Patients receiving antibiotics for some other reason

3.Patients with local skin infections at the site of surgery

4.Patients on steroids

5.Immunosuppressive disease(HIV)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Rate of Surgical Site Infection according to CDC definitionTimepoint: 30 Days
Secondary Outcome Measures
NameTimeMethod
Detecting potential risk factors in the development of surgical site infectionTimepoint: 30 Days
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