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Completed Not applicable Interventional Results available

Preventing Acute Chest Syndrome by Transfusion Feasibility Study

ClinicalTrials.gov ID: NCT00951808

Public ClinicalTrials.gov record NCT00951808. 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 Sep 3, 2026, 5:59 PM EDT

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

Official title

Preventing Acute Chest Syndrome by Transfusion Feasibility Study( PROACTIVE Feasibility Study)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Acute chest syndrome (ACS) is similar to severe pneumonia and is a common cause of hospitalizations for people with sickle cell disease (SCD). Blood transfusions are one treatment option for ACS. High levels of an enzyme called secretory phospholipase A2 (sPLA2) may be present in people before they develop ACS. This study will determine how well sPLA2 levels can predict the onset of ACS and whether identifying high sPLA2 levels allows enough time to prevent ACS with blood transfusions. Results from this study will help to determine the feasibility of conducting a larger study that would further examine the use of sPLA2 levels and blood transfusions to prevent ACS in people with SCD.

Study identification

NCT ID
NCT00951808
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Carelon Research
Other
Enrollment
237 participants

Conditions and interventions

Interventions

Biological · Behavioral

Eligibility (public fields only)

Age range
2 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
Jun 30, 2009
Primary completion
May 31, 2010
Completion
Jun 30, 2010
Last update posted
Apr 23, 2013

2009 – 2010

United States locations

U.S. sites
24
U.S. states
14
U.S. cities
17
Facility City State ZIP Site status
Children's Hospital and Research Center Oakland California
A.I. duPont Hospital for Children Wilmington Delaware
Children's National Medical Center Washington D.C. District of Columbia
Howard University Hospital Washington D.C. District of Columbia
Emory University School of Medicine Atlanta Georgia
Medical College of Georgia Augusta Georgia
Children's Memorial Hospital Chicago Illinois
University of Illinois Sickle Cell Center Chicago Illinois
Kosair Children's Hospital Louisville Kentucky
Johns Hopkins Baltimore Maryland
Boston Medical Center Boston Massachusetts
Brigham & Women's Hospital Boston Massachusetts
Children's Hospital Boston Boston Massachusetts
University of Mississippi Medical Center Jackson Mississippi
Interfaith Medical Center Brooklyn New York
New York Methodist Hospital Brooklyn New York
The University of North Carolina at Chapel Hill Chapel Hill North Carolina
Duke University Medical Center Durham North Carolina
Cincinnati Children's Hospital Medical Center Cincinnati Ohio
Nationwide Children's Hospital Columbus Ohio
Ohio State University Columbus Ohio
Children's Hospital of Philadelphia Philadelphia Pennsylvania
St. Christopher's Hospital for Children Philadelphia Pennsylvania
Virginia Commonwealth University Health Systems Richmond Virginia

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 NCT00951808, 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 Apr 23, 2013 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00951808 live on ClinicalTrials.gov.

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