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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Collection of Bone Marrow From Donors Treated With or Without Filgrastim

ClinicalTrials.gov ID: NCT01149096

Public ClinicalTrials.gov record NCT01149096. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 2, 2026, 10:12 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Comparison of Acute and Long-term Toxicities in Bone Marrow Donors With and Without G-CSF Treatment Prior to Harvest: A Companion Study to ASCT0631

Study identification

NCT ID
NCT01149096
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Children's Oncology Group
Network
Enrollment
13 participants

Conditions and interventions

Interventions

  • Bone Marrow Donation Procedure
  • Filgrastim Biological
  • Laboratory Biomarker Analysis Other

Procedure · Biological · Other

Eligibility (public fields only)

Age range
Not listed
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 13, 2010
Primary completion
Dec 13, 2011
Completion
Sep 29, 2016
Last update posted
Feb 25, 2020

2010 – 2016

United States locations

U.S. sites
22
U.S. states
17
U.S. cities
20
Facility City State ZIP Site status
UCSF Medical Center-Parnassus San Francisco California 94143
Children's Hospital Colorado Aurora Colorado 80045
Johns Hopkins All Children's Hospital St. Petersburg Florida 33701
Lurie Children's Hospital-Chicago Chicago Illinois 60611
Indiana University/Melvin and Bren Simon Cancer Center Indianapolis Indiana 46202
Riley Hospital for Children Indianapolis Indiana 46202
Norton Children's Hospital Louisville Kentucky 40202
Johns Hopkins University/Sidney Kimmel Cancer Center Baltimore Maryland 21287
C S Mott Children's Hospital Ann Arbor Michigan 48109
University of Mississippi Medical Center Jackson Mississippi 39216
Children's Mercy Hospitals and Clinics Kansas City Missouri 64108
Washington University School of Medicine St Louis Missouri 63110
New York Medical College Valhalla New York 10595
UNC Lineberger Comprehensive Cancer Center Chapel Hill North Carolina 27599
Rainbow Babies and Childrens Hospital Cleveland Ohio 44106
Nationwide Children's Hospital Columbus Ohio 43205
Children's Hospital of Philadelphia Philadelphia Pennsylvania 19104
Childrens Oncology Group Philadelphia Pennsylvania 19104
Children's Hospital of Pittsburgh of UPMC Pittsburgh Pennsylvania 15224
Vanderbilt University/Ingram Cancer Center Nashville Tennessee 37232
Primary Children's Hospital Salt Lake City Utah 84113
Virginia Commonwealth University/Massey Cancer Center Richmond Virginia 23298

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01149096, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 25, 2020 · Synced May 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01149096 live on ClinicalTrials.gov.

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