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

NCT02967432 · ClinicalTrials.gov registry record · Phase 2

Mupirocin to Reduce Staphylococcus Aureus Colonization in Infants Hospitalized in a NICU

A Phase 2 study of Staphylococcus, sponsored by Crouse Hospital.

Completed
Registry status
Phase 2
Development phase
216
Enrollment target
1
Study location

NCT02967432: Completed Phase 2 study of Staphylococcus, sponsored by Crouse Hospital.

NCT02967432 is a Phase 2 study of Staphylococcus that has completed, run by Crouse Hospital. The registered enrollment target is 216 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (62% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02967432, a Phase 2 study of Staphylococcus, has completed, sponsored by Crouse Hospital.

COMPLETED
Registry status
Phase 2
Development phase
216 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to determine whether or not mupirocin treatment results in S. aureus decolonization in affected NICU patients.

Primary Outcome

Compare the number of S. aureus patient colonization days between treatment versus control group

Conditions Studied

Interventions

  • DRUG Mupirocin Topical Ointment
  • DRUG Petroleum Jelly

Study Locations (1)

New York

  • Crouse Hospital - Neonatal Intensive Care Unit - Syracuse

Trial Details

FieldValue
Enrollment Target 216 participants
Start Date 2016-10
Est. Completion 2019-12
Phase Phase 2
Crouse Hospital

2 total trials

What the finished NCT02967432 record still lists

NCT02967432 is an interventional study that assigns participants to a tested intervention. The registered 216 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (62% higher).

The record links to 1 condition, with Staphylococcus appearing as the primary indexed condition, and to 2 interventions - of which Mupirocin Topical Ointment is the first listed.

NCT02967432 reports a single indexed study location in New York.

Frequently Asked Questions

What is clinical trial NCT02967432 about?

NCT02967432 is a clinical study titled "Mupirocin to Reduce Staphylococcus Aureus Colonization in Infants Hospitalized in a NICU". The purpose of this study is to determine whether or not mupirocin treatment results in S. aureus decolonization in affected NICU patients.

What is the current status of trial NCT02967432?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 216 participants. The study started on 2016-10. Estimated completion is 2019-12.

What conditions does trial NCT02967432 study?

This clinical trial studies the following conditions: Staphylococcus.

What interventions are being tested in trial NCT02967432?

The interventions under investigation include: Mupirocin Topical Ointment (DRUG), Petroleum Jelly (DRUG).

Who is sponsoring clinical trial NCT02967432?

This trial is sponsored by Crouse Hospital, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02967432 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT02967432's enrollment target sits among peer trials

216 286th of 2000 higher than 1,712 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02609685 · 216 participants · NA

    Active Surveillance of Papillary Thyroid Microcarcinoma

  • NCT04994873 · 216 participants · NA

    Skills to Enhance Positivity in Suicidal Youth

  • NCT05264779 · 216 participants · NA

    The Periviable GOALS Decision Support Tool

  • NCT05434130 · 216 participants · Phase 2

    Modulating Exercise Dosage to Improve Concussion Recovery

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02967432, the US trial registry maintained by the National Library of Medicine. NCT02967432 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.