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Clinical trialNCT01541319CompletedObservational

Mechanism and Repository Study for the Red Cell Storage Duration Study

SponsorCarelon ResearchEnrollment92Cardiac SurgeryErythrocyte Transfusion
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

A large multicenter randomized controlled trial of approximately 1700 critically ill patients' status post complex cardiac surgery with sternotomy, called the Red Cell Storage Duration Study (RECESS), is currently ongoing. In the RECESS trial, study groups are randomized to either RBCs of less than or equal to 10 days storage time or to greater than or equal to 21 days. The primary outcome of RECESS is a change in multiple organ dysfunction score. Secondary outcomes in RECESS include all cause 28-day mortality, mechanical ventilation free days, and other clinical outcomes. The RECESS study presents a unique opportunity to investigate mechanisms associated with RBC storage duration in the context of clinical outcomes for well-characterized surgical study groups. The ancillary study described here is called the Mechanism and Repository Study (MARS) for RECESS. The MARS study will analyze the most commonly reported and hypothesized mechanisms considered to be associated with the RBC storage lesion and adverse outcomes in critically ill patients. Laboratories with expertise in RBC function, nitric oxide mechanisms, the coagulation cascade, microparticle analysis and immunology will each examine hypotheses addressing mechanisms potentially able to relate storage time to clinical outcomes in RBC transfusion recipients. At the conclusion of the study, the results will provide a much better understanding of how RBC storage age affects recipient RBC function, coagulation parameters, microparticle load and immune modulation. Perhaps most importantly, this study will also develop a large sample repository for future analysis.

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

13 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Blood Systems Research Institute

    San Francisco, California, United States

  • Emory University

    Atlanta, Georgia, United States

  • Indiana/ohio Heart

    Fort Wayne, Indiana, United States

  • University of Iowa

    Iowa City, Iowa, United States

  • St. Elizabeth'S Medical Center

    Boston, Massachusetts, United States

  • University of Minnesota - Fairview

    Minneapolis, Minnesota, United States

  • Robert Wood Johnson Medial School

    New Brunswick, New Jersey, United States

  • Vanderbilt University

    Nashville, Tennessee, United States

  • University of Texas Southwestern

    Dallas, Texas, United States

  • Texas Heart Institute

    Houston, Texas, United States

  • Aurora St. Luke'S Medical Center

    Milwaukee, Wisconsin, United States

  • Froedtert Memorial Hospital

    Milwaukee, Wisconsin, United States

  • Aspirus Heart & Vascular Institute

    Wausau, Wisconsin, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Jul 2012
Primary completion
31 Aug 2016
Completion
31 Aug 2016
Last update posted
8 Sept 2016
Registered enrollment
92
Registry id
NCT01541319

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 4 Nov 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.