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NCT01484015 · ClinicalTrials.gov registry record · Phase 1

Prolonged or Standard Infusion of Cefepime Hydrochloride in Treating Patients With Febrile Neutropenia

A Phase 1 study, sponsored by Wake Forest University Health Sciences.

Completed
Registry status
Phase 1
Development phase
70
Enrollment target

NCT01484015: Completed Phase 1 study, sponsored by Wake Forest University Health Sciences.

NCT01484015 is a Phase 1 study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 70 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (17% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01484015, a Phase 1 study, has completed, sponsored by Wake Forest University Health Sciences.

COMPLETED
Registry status
Phase 1
Development phase
70 participants
Enrollment target

Study Summary

This randomized pilot clinical trial studies how well giving prolonged infusion compared to standard infusion of cefepime hydrochloride works in treating patients with febrile neutropenia. Giving cefepime hydrochloride over a longer period of time may be more effective than giving cefepime hydrochloride over the standard time.

Primary Outcome

Comparison between groups will be done using the chi square test. T-tests will be used for continues variables. Survival data will be estimated using the Kaplan-Meier method, with the formal test of group comparisons done using Cox's Proportional Hazards Model.

Interventions

  • DRUG cefepime hydrochloride

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2011-02
Est. Completion 2012-10
Phase Phase 1
Wake Forest University Health Sciences

1,140 total trials

What the finished NCT01484015 record still lists

NCT01484015 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 70 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (17% higher).

The record links to 0 conditions, and to 1 intervention - of which cefepime hydrochloride is the first listed.

NCT01484015 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01484015 about?

NCT01484015 is a clinical study titled "Prolonged or Standard Infusion of Cefepime Hydrochloride in Treating Patients With Febrile Neutropenia". This randomized pilot clinical trial studies how well giving prolonged infusion compared to standard infusion of cefepime hydrochloride works in treating patients with febrile neutropenia. Giving cefepime hydrochloride over a longer period of time may be more effective than giving cefepime hydrochlo...

What is the current status of trial NCT01484015?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 70 participants. The study started on 2011-02. Estimated completion is 2012-10.

What interventions are being tested in trial NCT01484015?

The interventions under investigation include: cefepime hydrochloride (DRUG).

Who is sponsoring clinical trial NCT01484015?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01484015's enrollment target sits among peer trials

70 749th of 2000 higher than 1,227 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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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Source: ClinicalTrials.gov NCT01484015, the US trial registry maintained by the National Library of Medicine. NCT01484015 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.