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NCT03268122 · ClinicalTrials.gov registry record · NA
Comparison of Standard Isolation With Targeted Isolation for Preventing Nosocomial Transmission of MRSA and VRE
A NA study, sponsored by Vanderbilt University Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 1,974
- Enrollment target
NCT03268122: Completed NA study, sponsored by Vanderbilt University Medical Center.
NCT03268122 is a NA study that has completed, run by Vanderbilt University Medical Center. The registered enrollment target is 1,974 participants, above the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (41% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03268122, a NA study, has completed, sponsored by Vanderbilt University Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 1,974 participants
- Enrollment target
Study Summary
Hospital-acquired infections are common and frequently lead to poor outcomes, including death, in affected patients. Two common organisms that cause infections in the hospital are methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus (VRE). One strategy used to prevent these infections is contact isolation of hospitalized patients with MRSA and/or VRE. It is unclear whether contact isolation decreases the rate of infection with MRSA and/or VRE. The CONTACT-PILOT study is designed to test the hypothesis that contact isolation decreases the rate of infection with MRSA and/or VRE in patients in the intensive care unit (ICU). The study will enroll all adults in the Medical ICU and will run between September 2017 and April 2018. During some months, all patients in the Medical ICU patients will be placed in isolation for MRSA or VRE if they have a current infection or colonization with either organism, or a recent history thereof. During other months, patients will only be placed in isolation for MRSA or VRE if they have an active, highly-transmissible infection with either organism, such as a pneumonia or an open, draining wound.
Primary Outcome
The primary endpoint is defined as an MRSA or VRE infection in a patient not currently diagnosed with or being treated for that infection at least 48 hours after admission to the study ICU and while the patient either remains in the study ICU or is within 48 hours of discharge or transfer from the study ICU, truncated at day 28 after enrollment. The composite rate will be reported in infections per 1000 patient-days.
Interventions
- OTHER Standard Contact Isolation
- OTHER Targeted Contact Isolation
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,974 participants |
| Start Date | 2017-09-01 |
| Est. Completion | 2018-05-30 |
| Phase | NA |
What the finished NCT03268122 record still lists
NCT03268122 is an interventional study that assigns participants to a tested intervention. Its 1,974 participants enrollment target places it among the larger protocols in the corpus, above the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (41% higher).
The record links to 0 conditions, and to 2 interventions - of which Standard Contact Isolation is the first listed.
NCT03268122 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03268122 about?
NCT03268122 is a clinical study titled "Comparison of Standard Isolation With Targeted Isolation for Preventing Nosocomial Transmission of MRSA and VRE". Hospital-acquired infections are common and frequently lead to poor outcomes, including death, in affected patients. Two common organisms that cause infections in the hospital are methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus (VRE). One strategy used to pre...
What is the current status of trial NCT03268122?
This trial is currently completed. It is a NA study. The enrollment target is 1,974 participants. The study started on 2017-09-01. Estimated completion is 2018-05-30.
What interventions are being tested in trial NCT03268122?
The interventions under investigation include: Standard Contact Isolation (OTHER), Targeted Contact Isolation (OTHER).
Who is sponsoring clinical trial NCT03268122?
This trial is sponsored by Vanderbilt University Medical Center, which has 677 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03268122's enrollment target sits among peer trials
1,974 54th of 2000 higher than 1,947 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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