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The Efficacy of Prophylactic Antibiotic Administration During Breast Cancer Surgery in Overweight Patients.

This study has been completed.
Information provided by (Responsible Party):
Bahadir M. Gulluoglu, M.D., Marmara University Identifier:
First received: July 24, 2006
Last updated: December 19, 2012
Last verified: December 2012
This is a single center trial to compare the rate of surgical site infection (SSI) in normal (BMI equal to or less than 25; Control Group)) and overweight (BMI over 25) women who are undergoing breast cancer surgery. The overweight patients are further randomized into two groups; in one group patients receive prophylactic antibiotics (ampicillin/sulbactam; Prophylaxis Group), in the other they do not (No Prophylaxis Group).

Condition Intervention Phase
Breast Cancer
Drug: Ampicillin/Sulbactam
Phase 4

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: Double Blind (Participant, Care Provider, Outcomes Assessor)
Primary Purpose: Prevention
Official Title: Phase IV Study of Determining the Efficacy of Ampicillin/Sulbactam Combination as Antibiotic Prophylaxis During Breast Cancer Surgery in Patients With a Body Mass Index (BMI) Over 25.

Resource links provided by NLM:

Further study details as provided by Marmara University:

Primary Outcome Measures:
  • Number of Patients With Body Mass Index (BMI) Over 25 Who Developed Surgical Site Infection (SSI) in Groups Who Received Antibiotic Prophylaxis (Prophylaxis Group) and no Prophylaxis (No Prophylaxis Group). [ Time Frame: 1 month ]

Secondary Outcome Measures:
  • Overall SSI-related Prophylaxis and Treatment Cost in Patients With BMI Over 25 Who Received Prophylaxis (Prophylaxis Group) and Not (No Prophylaxis Group). [ Time Frame: 1 month ]

Enrollment: 372
Study Start Date: October 2003
Study Completion Date: May 2010
Primary Completion Date: March 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: Prophylaxis Group
patients who are BMI over 25 and receiving ampicillin/sulbactam prophylaxis
Drug: Ampicillin/Sulbactam
Ampicillin/Sulbactam 1 gr, once within onr hour before surgery
Other Name: Ampisid 1 gr
No Intervention: No Prophylaxis Group
Patients who are BMI over 25 and do not receive antibiotic prophylaxis

Detailed Description:

CONTEXT Although breast surgery is regarded as clean surgery, the actual SSI rate is well above accepted range in various series. Retrospective studies showed BMI as one of the factors which may have caused increased SSI rate after breast cancer surgery. Yet, no prospective randomized study assessed the efficacy of chemoprophylaxis during breast surgery in overweight patients.

OBJECTIVE To compare the SSI rate between three groups of early stage breast cancer patients in which two are assigned according to randomization. First, patients are grouped into two according to their BMI. All patients (Control Group) with BMI equal to or below 25 do not receive any antibiotics as prophylaxis. Patients with a BMI above 25 are randomly assigned to receive a single dose prophylactic ampicillin /sulbactam combination before surgery (Prophylaxis Group) or not to receive chemoprophylaxis (No Prophylaxis Group).

DESIGN, SETTING AND PATIENTS Patient recruitment is still continuing after the study started in October 2003 in order to reach a sample size of 360 patients with BMI over 25. Advanced or distant metastatic stage, receiving neoadjuvant therapy, history of receiving antibiotics within prior 3 months, history of immunodeficiency, having a remote infection and history of reaction to treatment antibiotics are within the exclusion criteria.

INTERVENTIONS All patients are followed for 30 days postoperatively (once in a week at the original surgical unit). Patients and the investigator who inspects all wounds are blinded. Cost of SSI-related prophylaxis and treatments (including additional hospital visits after discharge, physician charges, additional antibiotics, wound management, other drugs and interventions etc) is calculated in each study group and compared with each other.


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Women at any age with early stage breast cancer (stage I-II) and American Society of Anesthesiologists (ASA) score of I-II.

Exclusion Criteria:

  • Ductal carcinoma in situ (DCIS; stage 0 cancer),
  • Advanced or distant metastatic stage,
  • Receiving any neoadjuvant therapy,
  • History of receiving any antibiotics within prior 3 months,
  • History of immunodeficiency,
  • Having a remote infection,
  • History of reaction to study antibiotics,
  • Denial of signing the consent form.
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Please refer to this study by its identifier: NCT00356148

Marmara University Hospital
Istanbul, Turkey, 34662
Sponsors and Collaborators
Marmara University
Study Chair: Bahadir M Gulluoglu, MD, FACS Marmara University School of Medicine, Department of General Surgery, Breast and Endocrine Surgery Unit
  More Information

Publications automatically indexed to this study by Identifier (NCT Number):
Responsible Party: Bahadir M. Gulluoglu, M.D., Prof Bahadir M Gulluoglu, MD, FACS, Marmara University Identifier: NCT00356148     History of Changes
Other Study ID Numbers: MAR-YC-2003-0111
Study First Received: July 24, 2006
Results First Received: April 20, 2012
Last Updated: December 19, 2012

Keywords provided by Marmara University:
breast cancer
breast surgery
clean wound

Additional relevant MeSH terms:
Breast Neoplasms
Neoplasms by Site
Breast Diseases
Skin Diseases
Anti-Bacterial Agents
Antibiotics, Antitubercular
Anti-Infective Agents
Antitubercular Agents
beta-Lactamase Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action processed this record on April 26, 2017