Skip to content

A Natural History Study of Bone and Mineral Disorders

A Natural History Study of Bone and Mineral Disorders

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00024804
Enrollment
1000
Registered
2001-10-01
Start date
2001-11-19
Completion date
Unknown
Last updated
2026-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Familial Tumoral Calcinosis, Osteomalacia, Tumor Induced Osteomalcia

Keywords

Natural History, skeletal diseases, Osteoporosis, Dysplasia, Osteomalacia, Bone Diseases, Skeletal Disease

Brief summary

This study has four objectives: 1) to provide investigators the opportunity to study bone specimens from patients with various skeletal diseases; 2) to treat patients with skeletal diseases at the NIH; 3) to expose NIH trainees to certain skeletal diseases; and 4) to gain more knowledge about skeletal diseases and stimulate further study of bone biology. Anyone with a disease that affects the skeleton may be eligible for this study. All evaluations, tests, procedures and treatments given study participants are used in the standard care of skeletal diseases. No experimental evaluations or treatments are offered. Patient evaluations include a medical history, review of medical records and routine physical examination. Based on the findings, other procedures may be recommended, including blood tests, urine tests, and imaging tests, such as X-rays, bone densitometry, bone scan, computed tomography (CT) and magnetic resonance imaging (MRI). Bone specimens from participants will be collected for research use. Specimens will be obtained from bone removed during a patient s planned surgical procedure performed for medical care, or patients may be requested to have a bone biopsy removal of a small piece of bone tissue as part of the patient evaluation procedure.

Detailed description

Study Description: To evaluate participants with bone and mineral disorders at the NIH Clinical Center and obtain tissue and clinical specimens from outside institutions Objectives: Primary Objective: Provide a protocol within which participants with common and rare disorders of bone and mineral metabolism can be studied, evaluated and treated at NIH. Secondary Objectives: To obtain tissue and clinical specimens (including but not limited to blood, urine, nucleic acids, skin and bone) and data collected at outside institutions and the NIH Clinical Center from participants with various bone and mineral disorders. Tertiary/Exploratory Objective: Generate a pool of participants with bone and mineral disorders, from which research questions could arise and future clinical research studies may be generated. Endpoints: Primary Endpoint: Medical evaluation with clinical assessments performed at time points specific to each participant s diagnosis. Analysis of research and participant outcome data will be performed. Secondary Endpoint: Genetic and/or biochemical assessments of surgical waste material from the NIH Clinical Center or other medical facilities. Tertiary/Exploratory Endpoint: Development of a database containing information from enrolled participants with bone and mineral disorders and annotated specimens and data.

Interventions

None listed

Sponsors

National Institute of Dental and Craniofacial Research (NIDCR)
Lead SponsorNIH

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Days to 100 Years
Healthy volunteers
No

Inclusion criteria

* INCLUSION CRITERIA: The study population will include participants with known or suspected bone disease and/or with a known or suspected disorder of mineral metabolism. To be eligible to participate in this study, an individual must meet all of the following criteria: 1. Age 1 day of life or older 2. Have a known or suspected bone disease, as demonstrated by any one of the following: a fracture, or abnormal bone findings on x-ray, CT scan, MRI, or bone densitometry, and/or a medical or family history consistent with or suggestive of a bone disease. 3. Have a known or suspected disorder of mineral metabolism, as demonstrated by any one of the following: laboratory measurement above or below the reference values for either blood or urine calcium, phosphorus, magnesium, parathyroid hormone or vitamin D, or other measures of mineral metabolism, and/or a medical or family history consistent with or suggestive of a disorder of mineral metabolism.

Exclusion criteria

1\. Participants unwilling or unable to abide by the procedures of the protocol.

Design outcomes

Primary

MeasureTime frameDescription
Collection of clinical and research specimens10 yearsSpecimens will be collected for creating better understanding of the disorders seen and for generating future research studies.

Countries

United States

Contacts

CONTACTElizabeth A Ferguson
elizabeth.ferguson@nih.gov(240) 687-3029
CONTACTKelly B Roszko, M.D.
kelly.roszko@nih.gov(301) 496-4563
PRINCIPAL_INVESTIGATORKelly B Roszko, M.D.

National Institute of Dental and Craniofacial Research (NIDCR)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 17, 2026