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Completed Phase 3 Interventional Results available

Red Cell Storage Duration Study

ClinicalTrials.gov ID: NCT00991341

Public ClinicalTrials.gov record NCT00991341. 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 Oct 22, 2026, 12:09 AM EDT

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

Brief summary

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

The RECESS study will compare the effects of transfusing red blood cell units stored \<= 10 days vs. red blood cell units stored \>= 21 days, in patients who are undergoing complex cardiac surgery and are likely to need a red blood cell transfusion. The primary hypothesis is that there is a clinically important difference between the effects of shorter-storage red cell units and longer-storage red cell units on clinical outcomes and mortality risk.

Study identification

NCT ID
NCT00991341
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Carelon Research
Other
Enrollment
1,481 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 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
Jan 2010 (Type not available)
Primary completion
Mar 2014 (Actual)
Completion
Mar 2014 (Actual)
Last update posted
Jun 9, 2015

2010 – 2014

United States locations

U.S. sites
33
U.S. states
17
U.S. cities
23
Facility City State ZIP Site status
University of Florida Gainesville Florida 32610 —
Emory University Atlanta Georgia 30322 —
St. Joseph Hospital Fort Wayne Indiana 46802 —
Indiana/Ohio Heart Fort Wayne Indiana 46804 —
University of Iowa Iowa City Iowa 52242 —
University of Maryland Baltimore Maryland 21201 —
Johns Hopkins University Baltimore Maryland 21287 —
Brigham & Women's Hospital Boston Massachusetts 02115 —
Children's Hospital Boston Boston Massachusetts 02115 —
Massachusetts General Hospital Boston Massachusetts 02115 —
St. Elizabeth's Medical Center Boston Massachusetts 02116 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
Baystate Medical Center Springfield Massachusetts 01199 —
Fairview Southdale Hospital/University of Minnesota Medical Center Fairview Minneapolis Minnesota 55455 —
Mayo Clinic Rochester Minnesota 55905 —
Robert Wood Johnson Medical School New Brunswick New Jersey 08903 —
Newark Beth Israel Deaconess Medical Center Newark New Jersey 07112 —
Columbia University Health Center New York New York 10032 —
Weill Cornell Medical School New York New York 10065 —
University of North Carolina at Chapel Hill Chapel Hill North Carolina 27599 —
Duke University Durham North Carolina 27713 —
Sanford Heart Center Fargo North Dakota 58122 —
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104 —
University of Pittsburgh Presbyterian and Shadyside Pittsburgh Pennsylvania 15213 —
UPMC-Mercy Hospital Pittsburgh Pennsylvania 15219 —
Vanderbilt University Medical Center Nashville Tennessee 37323 —
UT Southwestern Dallas Texas 75390 —
Texas Heart Institute Houston Texas 77030 —
Veterans Administration Puget Sound Seattle Washington 98108 —
Swedish Medical Center Seattle Washington 98195 —
Froedtert Memorial Lutheran Hospital Milwaukee Wisconsin 53201 —
Aurora St. Lukes Medical Center Milwaukee Wisconsin 53215 —
Aspirus Vascular Heart Center Wausau Wisconsin 54401 —

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 NCT00991341, 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 Jun 9, 2015 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00991341 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →