Rare Disease Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
If you have a bone or skeletal condition (affected participant):
- You have been diagnosed with, or are suspected to have, a skeletal disorder — particularly one that affects phosphate levels, causes unusual bone growth, or has an unknown cause — or you have had a pregnancy affected by skeletal findings
- You are willing and able to follow the study procedures for the full duration of the study
- You are at least 2 months old
- You are able to sign a consent form yourself, or a parent, guardian, or legal representative is available to sign on your behalf
If you are a healthy family member of someone enrolled (unaffected participant):
- You are a family member without a skeletal condition, related to someone already enrolled in the study
- You are willing and able to follow the study procedures for the full duration of the study
- You are at least 2 months old
- You are able to sign a consent form yourself, or a parent or guardian is available to sign on your behalf
Who may not be able to join:
- You are unwilling or unable to follow the study's required procedures
- You are currently pregnant
- As an affected participant: you do not show enough signs of, or risk factors for, a skeletal disorder (confirm with trial site)
- As an unaffected participant: you show any signs of a skeletal disorder
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Carlos R Ferreira Lopez, M.D., Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Phone: (301) 594-3391
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
To define or further define genetic etiologies of known and unknown skeletal disorders and create genotype-phenotype correlations when possible
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.