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NCT01523717 · ClinicalTrials.gov registry record

Procalcitonin Monitoring Sepsis Study

A clinical trial, sponsored by Brahms.

Completed
Registry status
858
Enrollment target

NCT01523717: Completed study, sponsored by Brahms.

NCT01523717 is a clinical trial that has completed, run by Brahms. The registered enrollment target is 858 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01523717 has completed, sponsored by Brahms.

COMPLETED
Registry status
858 participants
Enrollment target

Study Summary

The purpose of this study is to investigate the relationship between a procalcitonin decrease over 72 hours and outcome in patients who have severe sepsis or septic shock.

Primary Outcome

participants will be followed up for 28 days

Trial Details

FieldValue
Enrollment Target 858 participants
Start Date 2011-12
Est. Completion 2014-03
Brahms

5 total trials

What the finished NCT01523717 record still lists

NCT01523717 is an observational study that tracks outcomes without assigning an intervention. The registered 858 participants enrollment target is mid-sized for trials with a published cap.

The record links to 0 conditions, and to 0 interventions.

NCT01523717 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01523717 about?

NCT01523717 is a clinical study titled "Procalcitonin Monitoring Sepsis Study". The purpose of this study is to investigate the relationship between a procalcitonin decrease over 72 hours and outcome in patients who have severe sepsis or septic shock.

What is the current status of trial NCT01523717?

This trial is currently completed. The enrollment target is 858 participants. The study started on 2011-12. Estimated completion is 2014-03.

Who is sponsoring clinical trial NCT01523717?

This trial is sponsored by Brahms, which has 5 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT01523717, the US trial registry maintained by the National Library of Medicine. NCT01523717 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.