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NCT00490256 · ClinicalTrials.gov registry record · NA

Modified Perfusion for Neonatal Aortic Arch Reconstruction

A NA study, sponsored by Emory University.

Completed
Registry status
NA
Development phase
14
Enrollment target

NCT00490256: Completed NA study, sponsored by Emory University.

NCT00490256 is a NA study that has completed, run by Emory University. The registered enrollment target is 14 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00490256, a NA study, has completed, sponsored by Emory University.

COMPLETED
Registry status
NA
Development phase
14 participants
Enrollment target

Study Summary

Even though the lower part of the body does receive some blood supply during Cardiopulmonary Bypass(CPB) surgery, it may not be enough. As a result of this lowered blood supply, there are complications associated with CPB and clamping of the aorta. These include complications with the stomach, intestines and kidneys. The hypotheses of this study are that increased lower body perfusion during aortic arch reconstruction will decrease intestinal ischemia and the incidence of necrotizing enterocolitis, improve renal function in the postoperative period, and shorten both intensive care unit and hospital length of stay. The purpose of this research study is to provide the lower part of the body and its organs with possibly more blood supply with a modified form of cardiopulmonary bypass and see if this additional blood supply helps to decrease complications of the kidney, stomach and intestines.

Interventions

  • PROCEDURE Modified Selective Cerebral Perfusion

Trial Details

FieldValue
Enrollment Target 14 participants
Start Date 2007-06
Est. Completion 2010-06
Phase NA
Emory University

1,208 total trials

What the finished NCT00490256 record still lists

NCT00490256 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 14 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 1 intervention - of which Modified Selective Cerebral Perfusion is the first listed.

NCT00490256 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00490256 about?

NCT00490256 is a clinical study titled "Modified Perfusion for Neonatal Aortic Arch Reconstruction". Even though the lower part of the body does receive some blood supply during Cardiopulmonary Bypass(CPB) surgery, it may not be enough. As a result of this lowered blood supply, there are complications associated with CPB and clamping of the aorta. These include complications with the stomach, intes...

What is the current status of trial NCT00490256?

This trial is currently completed. It is a NA study. The enrollment target is 14 participants. The study started on 2007-06. Estimated completion is 2010-06.

What interventions are being tested in trial NCT00490256?

The interventions under investigation include: Modified Selective Cerebral Perfusion (PROCEDURE).

Who is sponsoring clinical trial NCT00490256?

This trial is sponsored by Emory University, which has 1,208 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00490256's enrollment target sits among peer trials

14 1909th of 2000 higher than 90 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

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Source: ClinicalTrials.gov NCT00490256, the US trial registry maintained by the National Library of Medicine. NCT00490256 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.