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Routine Preoperative Antibiotic Prophylaxis in Modified Radical Mastectomy

U

University of the Philippines

Status and phase

Completed
Phase 3

Conditions

Surgical Infection

Treatments

Procedure: Cefazolin
Procedure: Sterile water

Study type

Interventional

Funder types

Other

Identifiers

NCT01558986
NIH 2007-07-10-02

Details and patient eligibility

About

This is a randomized, double blinded, placebo-controlled trial on the routine use of preoperative antibiotic prophylaxis in modified radical mastectomy to evaluate the efficacy of preoperative prophylactic antibiotics in the prevention of surgical site infection (SSI) in patients undergoing modified radical mastectomy (MRM) for breast care.

Full description

A randomized, double blinded, placebo-controlled trial on the routine use of preoperative antibiotic prophylaxis in modified radical mastectomy to evaluate the efficacy of preoperative prophylactic antibiotics in the prevention of surgical site infection (SSI) in patients undergoing modified radical mastectomy (MRM) for breast care.

Women with breast cancer who will undergo elective MRM were recruited for the study. Excluded were patients with significant co-morbid factors, for simultaneous breast reconstruction or bilateral oophorectomy, with intake of antibiotics within one week, with known allergy to cephalosporins, and those with local infection. Patients were randomized to receive either transvenous cefazolin 1 gram or sterile water only within 30 minutes prior to skin incision. Standard skin preparation and operative technique for MRM were carried out. Wounds were assessed for the presence of SSI and other complications weekly for 30 days.

Enrollment

254 patients

Sex

Female

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Women with histologically diagnosed breast cancer of age group 18-80 years old, ECOG 0-1, clinical stage I to IIIB, admitted to the surgery ward, who were scheduled for elective MRM.

Exclusion criteria

  • Women with significant co-morbid factors (diabetes mellitus, severe malnutrition, corticosteroid therapy), those scheduled for simultaneous breast reconstruction or bilateral oophorectomy, with intake of antibiotics within one week prior to surgery, with known allergy to cephalosporins, and those with local infection.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

254 participants in 2 patient groups, including a placebo group

Treatment Arm
Active Comparator group
Description:
Patients to receive intravenous cefazolin 1 gram within 30 minutes prior to skin incision
Treatment:
Procedure: Cefazolin
Placebo Arm
Placebo Comparator group
Description:
Patients to receive sterile water only within 30 minutes prior to skin incision
Treatment:
Procedure: Sterile water

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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