Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01537783 · ClinicalTrials.gov registry record · Phase 4

Evaluation of a Staphylococcus Eradication Protocol for Patients Who Present to the ED With Cutaneous Abscess

A Phase 4 study, sponsored by Tufts Medical Center.

Completed
Registry status
Phase 4
Development phase
50
Enrollment target

NCT01537783 is a Phase 4 study that has completed, run by Tufts Medical Center. The registered enrollment target is 50 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01537783, a Phase 4 study, has completed, sponsored by Tufts Medical Center.

COMPLETED
Registry status
Phase 4
Development phase
50 participants
Enrollment target

Study Summary

In this study, the investigators will enroll patients who present to the emergency department with abscesses to the study. The patients will be randomly selected to either have the standard of care, which includes the standard drainage of the abscess and then usually a follow-up visit to recheck the wound, or to have the standard of care plus instructions to use a topical scrub of a soap called chlorhexidine once a day for five days and twice daily application of a topical antibiotic ointment called mupirocin to the nasal passages for five days. The investigators will then call back the patients at 7 days, 14 days (if in the treatment arm), 3 months and 6 months, to ask if they have had any recurrence of abscess formation. The study hypothesis is that the patients who have undergone the decontamination protocol will have fewer subsequent infections.

Interventions

  • DRUG Mupirocin
  • DRUG Chlorhexidine gluconate

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2011-09
Est. Completion 2013-09
Phase Phase 4

Sponsor

Tufts Medical Center

169 total trials

What the Registry Record Tells You About NCT01537783

The ClinicalTrials.gov registry entry for NCT01537783 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Tufts Medical Center, which has 169 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Mupirocin is the first listed.

NCT01537783 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01537783 about?

NCT01537783 is a clinical study titled "Evaluation of a Staphylococcus Eradication Protocol for Patients Who Present to the ED With Cutaneous Abscess". In this study, the investigators will enroll patients who present to the emergency department with abscesses to the study. The patients will be randomly selected to either have the standard of care, which includes the standard drainage of the abscess and then usually a follow-up visit to recheck the...

What is the current status of trial NCT01537783?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 50 participants. The study started on 2011-09. Estimated completion is 2013-09.

What interventions are being tested in trial NCT01537783?

The interventions under investigation include: Mupirocin (DRUG), Chlorhexidine gluconate (DRUG).

Who is sponsoring clinical trial NCT01537783?

This trial is sponsored by Tufts Medical Center, which has 169 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.