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NCT00228813 · ClinicalTrials.gov registry record · NA

G-CSF PMRD: Granulocyte Colony Stimulating Factor (G-CSF) Stimulated Bone Marrow and In Vivo T-Cell Depletion in Patients With Hematologic Malignancies or Bone Marrow Failure Syndrome

A NA study, sponsored by Emory University.

Terminated
Registry status
NA
Development phase
8
Enrollment target

NCT00228813: Clinical Trial NA study, sponsored by Emory University.

NCT00228813 is a NA study that was terminated before completion, run by Emory University. The registered enrollment target is 8 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

NCT00228813, a NA study, was terminated before completion, sponsored by Emory University.

TERMINATED
Registry status
NA
Development phase
8 participants
Enrollment target

Study Summary

The purposes of this study are: * To examine the engraftment rate in patients receiving in vivo T-cell-depleted G-CSF stimulated bone marrow from partially mismatched related donors. * To evaluate the incidence and severity of acute and chronic graft-versus-host disease in patients receiving in vivo T-cell-depleted G-CSF stimulated bone marrow from partially mismatched related donors.

Primary Outcome

The number of participants who received in vivo T-cell-depleted G-CSF stimulated bone marrow from partially mismatched related donor who reached engraftment by Day 45.

Interventions

  • DRUG Granulocyte Colony Stimulating Factor

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2004-04
Est. Completion 2015-01
Phase NA
Emory University

1,208 total trials

Why NCT00228813 stopped before completion

NCT00228813 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 8 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 Granulocyte Colony Stimulating Factor is the first listed.

NCT00228813 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00228813 about?

NCT00228813 is a clinical study titled "G-CSF PMRD: Granulocyte Colony Stimulating Factor (G-CSF) Stimulated Bone Marrow and In Vivo T-Cell Depletion in Patients With Hematologic Malignancies or Bone Marrow Failure Syndrome". The purposes of this study are: * To examine the engraftment rate in patients receiving in vivo T-cell-depleted G-CSF stimulated bone marrow from partially mismatched related donors. * To evaluate the incidence and severity of acute and chronic graft-versus-host disease in patients receiving in viv...

What is the current status of trial NCT00228813?

This trial is currently terminated. It is a NA study. The enrollment target is 8 participants. The study started on 2004-04. Estimated completion is 2015-01.

What interventions are being tested in trial NCT00228813?

The interventions under investigation include: Granulocyte Colony Stimulating Factor (DRUG).

Who is sponsoring clinical trial NCT00228813?

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 NCT00228813's enrollment target sits among peer trials

8 1976th of 2000 higher than 19 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 NCT00228813, the US trial registry maintained by the National Library of Medicine. NCT00228813 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.