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Completed No phase listed Observational

Procalcitonin Monitoring Sepsis Study

ClinicalTrials.gov ID: NCT01523717

Public ClinicalTrials.gov record NCT01523717. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jun 26, 2026, 8:38 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Procalcitonin Decrease Over 72 Hours and Outcome in Patients With Severe Sepsis or Septic Shock

Study identification

NCT ID
NCT01523717
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Brahms AG
Industry
Enrollment
858 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 30, 2011
Primary completion
Feb 28, 2014
Completion
Feb 28, 2014
Last update posted
Mar 16, 2015

2011 – 2014

United States locations

U.S. sites
13
U.S. states
9
U.S. cities
10
Facility City State ZIP Site status
University of California Davis Health System Sacramento California 95817
Northwestern University Chicago Illinois 60611
Beth Israel Deaconess Medical Center Boston Massachusetts 02215
Saint Vincent Hospital Worcester Massachusetts 01608
Detroit Receiving Hospital Detroit Michigan 48201
Sinai Grace Hospital Detroit Michigan 48201
Henry Ford Health System Detroit Michigan 48202
University of Mississippi Medical Center Jackson Mississippi 39216
New York Methodist Hospital New York New York 11215
Stony Brook University New York New York 11794
Carolinas Medical Center Charlotte North Carolina 28203
Hospital of the University of Pennsylvania Philadelphia Pennsylvania 19104
Vanderbilt University Medical Center Nashville Tennessee 37232

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01523717, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 16, 2015 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01523717 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →