Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05796557 · ClinicalTrials.gov registry record · Phase 4

ECMO Hemostatic Transfusions in Children

A Phase 4 study, sponsored by Yale University.

Completed
Registry status
Phase 4
Development phase
50
Enrollment target

NCT05796557: Completed Phase 4 study, sponsored by Yale University.

NCT05796557 is a Phase 4 study that has completed, run by Yale University. The registered enrollment target is 50 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05796557, a Phase 4 study, has completed, sponsored by Yale University.

COMPLETED
Registry status
Phase 4
Development phase
50 participants
Enrollment target

Study Summary

Critically ill children supported by extracorporeal membrane oxygenation (ECMO) receive large volumes of prophylactic platelet transfusions to prevent bleeding. However, mounting evidence has demonstrated significant morbidity and mortality associated with these transfusions. The ECmo hemoSTAtic Transfusions In Children (ECSTATIC) pilot trial will test two different platelet transfusion strategies, based on two different platelet counts thresholds, one high (higher platelet transfusion strategy) and one low (lower platelet transfusion strategy). The pilot will gather the necessary information to perform a full trial which will provide a better understanding of how to transfuse platelets to children supported by ECMO and reduce the associated morbidity.

Primary Outcome

The total dose (in mL/kg/day) will be computed by the research team, by dividing the total platelet transfusion volume by the patient's weight at admission and the number of days of intervention.

Interventions

  • BIOLOGICAL Platelet Transfusion

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2023-12-12
Est. Completion 2025-03-25
Phase Phase 4
Yale University

1,492 total trials

What the finished NCT05796557 record still lists

NCT05796557 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (90% lower).

The record links to 0 conditions, and to 1 intervention - of which Platelet Transfusion is the first listed.

NCT05796557 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05796557 about?

NCT05796557 is a clinical study titled "ECMO Hemostatic Transfusions in Children". Critically ill children supported by extracorporeal membrane oxygenation (ECMO) receive large volumes of prophylactic platelet transfusions to prevent bleeding. However, mounting evidence has demonstrated significant morbidity and mortality associated with these transfusions. The ECmo hemoSTAtic Tra...

What is the current status of trial NCT05796557?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 50 participants. The study started on 2023-12-12. Estimated completion is 2025-03-25.

What interventions are being tested in trial NCT05796557?

The interventions under investigation include: Platelet Transfusion (BIOLOGICAL).

Who is sponsoring clinical trial NCT05796557?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05796557's enrollment target sits among peer trials

50 1255th of 2000 higher than 678 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00200889 · 50 participants · Early Phase 1

    Mapping Auricular Vagus Nerve Circuitry

  • NCT00409435 · 50 participants · Phase 2

    A Study of Pyridostigmine in Postural Tachycardia Syndrome

  • NCT01202305 · 50 participants

    The Use of Lymph Node Biopsies to Support HIV Pathogenesis Studies

  • NCT01225913 · 50 participants · Phase 4

    Mechanism(s) of Airflow Limitation During Exacerbation of Asthma

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT05796557, the US trial registry maintained by the National Library of Medicine. NCT05796557 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.