Trial record 5 of 6 for:
"Albrights hereditary osteodystrophy"
Study of the Regulation of Parathyroid Hormone Secretion in Pseudohypoparathyroidism
This study has been completed.
Sponsor:
Collaborator:
University of California, Los Angeles
Information provided by:
Office of Rare Diseases (ORD)
ClinicalTrials.gov Identifier:
NCT00004661
First received: February 24, 2000
Last updated: June 23, 2005
Last verified: December 2001
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Purpose
OBJECTIVES:
Determine the relationship between serum calcium concentrations and parathyroid hormone secretion in patients with pseudohypoparathyroidism.
| Condition |
|---|
|
Pseudohypoparathyroidism |
| Study Type: | Observational |
| Study Design: | Primary Purpose: Screening |
Further study details as provided by Office of Rare Diseases (ORD):
Eligibility| Ages Eligible for Study: | 12 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
PROTOCOL ENTRY CRITERIA:
--Disease Characteristics-- Pseudohypoparathyroidism, i.e.: Renal resistance to parathyroid hormone OR Albright hereditary osteodystrophy No other illness unless related to pseudohypoparathyroidism No pregnant women
Contacts and Locations
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00004661 History of Changes |
| Other Study ID Numbers: | 199/11909, UCLA-541 |
| Study First Received: | February 24, 2000 |
| Last Updated: | June 23, 2005 |
| Health Authority: | United States: Federal Government |
Keywords provided by Office of Rare Diseases (ORD):
|
endocrine disorders pseudohypoparathyroidism rare disease |
Additional relevant MeSH terms:
|
Pseudohypoparathyroidism Pseudopseudohypoparathyroidism Bone Diseases, Metabolic Bone Diseases Musculoskeletal Diseases |
Metal Metabolism, Inborn Errors Metabolism, Inborn Errors Genetic Diseases, Inborn Calcium Metabolism Disorders Metabolic Diseases |
ClinicalTrials.gov processed this record on May 22, 2013