CClinicalTrials.gg
CompletedNCT00594295Updated Oct 5, 2015

Follow-up of Bone Quality in Long-Term Bone Marrow Transplant Survivors

An observational study in Osteoporotic Fractures, sponsored by University of Wisconsin, Madison. Completed at 1 site in United States. Per ClinicalTrials.gov, last updated 2015-10-05.

Sponsored by University of Wisconsin, Madison · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
15
Sex
All
01

Study summary

Brittle and broken bones can occur after organ transplantation. However, the long-term effects of bone marrow transplantation on bone health and the risk of breaking bones are not well understood. This study will help to assess how common it is for those who have received a bone marrow transplant to have fractures. It will also investigate blood tests related to bone health. This will be done by measuring bone mineral density and obtaining blood tests.

02

Conditions studied

  • Osteoporotic Fractures

Browse trials for

03

In context

Osteoporotic Fractures

91 studies on the registry are indexed under Osteoporotic Fractures; 22 are open to participants now.

This study's planned enrollment of 15 is below the median of 264 across 37 observational studies indexed under Osteoporotic Fractures.

Browse Osteoporotic Fractures studies →

Lead sponsor

University of Wisconsin, Madison is the lead sponsor of 1,161 studies on the registry; 182 are open to participants now.

Of its 151 completed or terminated interventional studies of FDA-regulated products, 114 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Bone marrow transplant patients at least 6 years post transplant

Inclusion criteria

  • Participation in the initial "Assessment of skeletal status following allogeneic bone marrow transplantation" Study (HSC97-632-408).
  • Able and willing to sign informed consent.

Exclusion criteria

Exclusion Criteria:

  • All of the contacted long-term BMT survivors that are willing to participate will be included in this study
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
15 participants (estimated)
Biospecimen retention
Samples without dna
06

Study locations

1 site
  • University of Wisconsin Hospitals and Clinics
    Madison, Wisconsin 53705, United States
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 5, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00594295
Lead sponsor
University of Wisconsin, Madison
Responsible party
Sponsor
First posted
Jan 15, 2008
Start date
Jun 2007
Primary completion
Jul 2008
Completion
Jul 2008
Last update
Oct 5, 2015

Study contacts

Neil C Binkley, MD
principal investigator · University of Wisconsin - Institute on Aging

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2010. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion