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NCT01211366 · ClinicalTrials.gov registry record · NA

Use of Cell Salvage Post-operatively in Infants to Decrease Use of Allogeneic Blood Product Transfusions

A NA study, sponsored by University of Rochester.

Completed
Registry status
NA
Development phase
106
Enrollment target

NCT01211366 is a NA study that has completed, run by University of Rochester. The registered enrollment target is 106 participants.

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The verdict

NCT01211366, a NA study, has completed, sponsored by University of Rochester.

COMPLETED
Registry status
NA
Development phase
106 participants
Enrollment target

Study Summary

Transfusion of washed intra-operative cell salvage post-operatively in the PCICU can be performed safely without increased risk of bleeding or release of inflammatory mediators. This will reduce the need for allogeneic blood products as well as crystalloid and colloid infusions and thus decrease the length of ventilation and intensive care duration for these infants.

Interventions

  • OTHER Cell Saver RBCs
  • OTHER Conventional volume infusion

Trial Details

FieldValue
Enrollment Target 106 participants
Start Date 2010-10
Est. Completion 2011-12
Phase NA

Sponsor

University of Rochester

636 total trials

What the Registry Record Tells You About NCT01211366

The ClinicalTrials.gov registry entry for NCT01211366 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 106 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Rochester, which has 636 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Cell Saver RBCs is the first listed.

NCT01211366 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01211366 about?

NCT01211366 is a clinical study titled "Use of Cell Salvage Post-operatively in Infants to Decrease Use of Allogeneic Blood Product Transfusions". Transfusion of washed intra-operative cell salvage post-operatively in the PCICU can be performed safely without increased risk of bleeding or release of inflammatory mediators. This will reduce the need for allogeneic blood products as well as crystalloid and colloid infusions and thus decrease the...

What is the current status of trial NCT01211366?

This trial is currently completed. It is a NA study. The enrollment target is 106 participants. The study started on 2010-10. Estimated completion is 2011-12.

What interventions are being tested in trial NCT01211366?

The interventions under investigation include: Cell Saver RBCs (OTHER), Conventional volume infusion (OTHER).

Who is sponsoring clinical trial NCT01211366?

This trial is sponsored by University of Rochester, which has 636 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.