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NCT01965730 · ClinicalTrials.gov registry record · Early Phase 1

Dosing of Amicar and Measure of Fibrinolysis by TEG During Cardiac Surgery

A Early Phase 1 study, sponsored by University of Pennsylvania.

Terminated
Registry status
Early Phase 1
Development phase
8
Enrollment target

NCT01965730: Clinical Trial Early Phase 1 study, sponsored by University of Pennsylvania.

NCT01965730 is a Early Phase 1 study that was terminated before completion, run by University of Pennsylvania. The registered enrollment target is 8 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01965730, a Early Phase 1 study, was terminated before completion, sponsored by University of Pennsylvania.

TERMINATED
Registry status
Early Phase 1
Development phase
8 participants
Enrollment target

Study Summary

This study hopes to determine the optimal antifibrinolytic dosing to decrease bleeding and blood transfusion after cardiac surgery without increasing adverse events

Interventions

  • DRUG epsilon-aminocaproic acid (EACA)

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2013-01
Est. Completion 2014-06
Phase Early Phase 1

Sponsor

University of Pennsylvania

1,423 total trials

What the Registry Record Tells You About NCT01965730

The ClinicalTrials.gov registry entry for NCT01965730 describes a study currently listed as terminated, categorized as Early Phase 1. The registered enrollment target is 8 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Pennsylvania, which has 1,423 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which epsilon-aminocaproic acid (EACA) is the first listed.

NCT01965730 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01965730 about?

NCT01965730 is a clinical study titled "Dosing of Amicar and Measure of Fibrinolysis by TEG During Cardiac Surgery". This study hopes to determine the optimal antifibrinolytic dosing to decrease bleeding and blood transfusion after cardiac surgery without increasing adverse events

What is the current status of trial NCT01965730?

This trial is currently terminated. It is a Early Phase 1 study. The enrollment target is 8 participants. The study started on 2013-01. Estimated completion is 2014-06.

What interventions are being tested in trial NCT01965730?

The interventions under investigation include: epsilon-aminocaproic acid (EACA) (DRUG).

Who is sponsoring clinical trial NCT01965730?

This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.

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

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, the data changelog, or report a data error.