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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02348866
Other study ID # Pro#00041187
Secondary ID
Status Completed
Phase N/A
First received January 23, 2015
Last updated January 13, 2016
Start date January 2015
Est. completion date January 2016

Study information

Verified date January 2016
Source Greenville Health System
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This study will determine if there is a difference in bacterial contamination (CFU/cm2) between obstetric resident surgical scrubs donned at home and those donned at the hospital.


Description:

An area of potential provider-to-patient contamination, and therefore intervention, is in health care worker attire and laundering practices. For providers who work in the operating room or labor & delivery suites, this uniform usually comprises hospital-issued surgical scrubs. To the best of our knowledge, no study has measured the difference in bacterial contamination on surgical scrubs vis-a-vis the two variables most directly affected by hospital policies for surgical attire: site of scrub laundering and site where scrubs were first put on. In addition, no study has measured the prevalence of antibiotic-resistant organisms on surgical scrubs in the obstetric setting. Our primary objective is to measure the difference in bacterial contamination (CFU/cm2) between home-laundered/home-donned scrubs ("home/home," group 1), hospital-laundered/home-donned scrubs ("hospital/home," group 2), home-laundered/hospital-donned scrubs ("home/hospital," group 3), and hospital-laundered/hospital-donned scrubs ("hospital/hospital," group 4) in the obstetric setting. Our secondary objective is to determine the prevalence of antibiotic-resistant organisms on surgical scrubs in the obstetric setting.


Recruitment information / eligibility

Status Completed
Enrollment 18
Est. completion date January 2016
Est. primary completion date July 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- ob-gyn residents assigned to labor and delivery during the day on one of seven rotation blocks

Exclusion Criteria:

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Other:
method of laundering and donning scrubs


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Greenville Health System

Outcome

Type Measure Description Time frame Safety issue
Primary difference in bacterial contamination between scrubs donned at home and those put on in the hospital, when location of laundering is considered (as determined by (CFU/cm2) 4 days of randomization per subject 4 days No
Secondary Prevalence of antibiotic resistant Staphylococcus aureus on surgical scrubs in the obstetric setting 4 days of randomization per subject 4 days No
See also
  Status Clinical Trial Phase
Completed NCT04927806 - The Effectiveness of Antimicrobial Breathing System on the Presence of Multidrug-resistant Organisms N/A
Completed NCT01594580 - Contamination of Hospital Scrubs N/A