Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
50 participants
INTERVENTIONAL
2003-07-31
2006-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Interventions
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Perindopril
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Unstable renal function
* Hyperkaliemia
2 Years
16 Years
ALL
No
Sponsors
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Institut de Recherches Internationales Servier
OTHER
Principal Investigators
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Patrick Niaudet, Pr
Role: STUDY_CHAIR
Hôpital Necker-Enfants Malades, Paris, France
Locations
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Hôpital Necker Enfants Malades
Paris, , France
Countries
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Other Identifiers
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CL2-90652-001
Identifier Type: -
Identifier Source: org_study_id
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