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Clinical Trials/NCT00646828
NCT00646828
Completed
Not Applicable

Cardiovascular Evaluation of a Rare Condition With Hyperaldosteronism Without Hypertension: PHA 1

Assistance Publique - Hôpitaux de Paris1 site in 1 country98 target enrollmentMay 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pseudohypoaldosteronism Type 1
Sponsor
Assistance Publique - Hôpitaux de Paris
Enrollment
98
Locations
1
Primary Endpoint
Cardiac or vascular abnormality at ultrasound or NMR evaluation
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

Vascular and cardiac alterations are associated with aldosterone effects are evidenced in experimental models and aldosterone receptor blockade is of clear benefit in cardiac disease (heart failure). The study aims at assessing vascular and cardiac alterations in adults with a chronic increase in circulating aldosterone without hypertension. The investigated population will be patients with a rare disease, pseudohypoaldosteronism type 1, due to heterozygous inactivating mutations of the mineralocorticoid receptor.

Detailed Description

The study includes adult patients with mineralocorticoid receptor mutation as compared with not affected relatives. It includes also relatives of adult relative of patients with PHA1 in whom no mutation was found. Cardiovascular evaluation is conducted with cardiac and vascular ultrasound assessment and cardiac NMR, ambulatory blood pressure measurement. Protocol duration is 2 days . Detailed genetic study is conducted in family without identified mutation in MINERALORECEPTOR.

Registry
clinicaltrials.gov
Start Date
May 2008
End Date
May 2011
Last Updated
14 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Cardiac or vascular abnormality at ultrasound or NMR evaluation

Time Frame: day one

Secondary Outcomes

  • Extracellular volume, biology, autonomic nervous system abnormality(day one + day two)
  • New gene responsible for PHA1(day one)

Study Sites (1)

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