ClinicalTrials.gov record
Terminated Not applicable Interventional Results available

Safety and Efficacy Study of Autologous Concentrated Bone Marrow Aspirate (cBMA) for Critical Limb Ischemia (CLI)

ClinicalTrials.gov ID: NCT01049919

Public ClinicalTrials.gov record NCT01049919. 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 19, 2026, 7:48 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

MarrowStim PAD Kit for the Treatment of Critical Limb Ischemia (CLI) in Subjects With Severe Peripheral Arterial Disease (PAD)

Study identification

NCT ID
NCT01049919
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
Zimmer Biomet
Industry
Enrollment
153 participants

Conditions and interventions

Interventions

  • Bone marrow concentration device Device
  • Placebo procedure (sham) Procedure

Device · Procedure

Eligibility (public fields only)

Age range
21 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
May 31, 2010
Primary completion
May 31, 2016
Completion
Jan 31, 2020
Last update posted
May 27, 2021

2010 – 2020

United States locations

U.S. sites
25
U.S. states
20
U.S. cities
23
Facility City State ZIP Site status
Central Arkansas Veterans Healthcare System Little Rock Arkansas 72205
University of California-Davis Medical Center Sacramento California 95817
University of Miami Miami Florida 33136
Piedmont Hospital Atlanta Georgia 30309
Northwestern University Chicago Illinois 60611
Indiana University School of Medicine Indianapolis Indiana 46202
University of Iowa Hospitals and Clinics Iowa City Iowa 52242
University of Louisville Louisville Kentucky 40202
Tufts Medical Center Boston Massachusetts 02111
UMass Memorial Health Care Worcester Massachusetts 01655
Spectrum Health Grand Rapids Michigan 49503
Saint Luke's Hospital Kansas City Missouri 64111
Nebraska-Western Iowa VA Healthcare System Omaha Nebraska 68105
Holy Name Medical Center Teaneck New Jersey 07666
The Mount Sinai Hospital New York New York 10029
Weill Cornell Medical College / New York-Presbyterian Hospital New York New York 10065
University Hospitals Cleveland Medical Center Cleveland Ohio 44106
The Cleveland Clinic Cleveland Ohio 44195
Remington-Davis Columbus Ohio 43215
Temple University Hospital Philadelphia Pennsylvania 19140
VA Pittsburgh Healthcare System Pittsburgh Pennsylvania 15240
The Methodist Hospital Houston Texas 77030
University of Virginia Hospital Charlottesville Virginia 22908
Providence Sacred Heart Medical Center Spokane Washington 99204
Aurora St. Luke's Medical Center Milwaukee Wisconsin 53215

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 NCT01049919, 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 May 27, 2021 · Synced May 19, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01049919 live on ClinicalTrials.gov.

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