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OpenTrials
Completed

NCT Number: NCT00202592

S90652 in Paediatric Hypertension

The aim of the study is to assess the long-term safety and effects on blood pressure of a paediatric formulation of perindopril in hypertensive children

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Key information

Age range

30 month–17 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Hôpital Necker Enfants Malades

Paris, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Hypertensive children, who have been treated for four months at least with S90652, with safety and efficacy

Exclusion criteria

  • Poorly controlled hypertension
  • Girls with signs of pubescence

Treatment and study plan

perindopril

Drug

Primary outcomes

  1. Clinical safety assessed from the patient's (parents) complaints and clinical follow-up

Secondary outcomes

  1. Blood pressure

Sponsors and collaborators

Lead sponsor

Institut de Recherches Internationales Servier

Other

Registry information

Official study title

Safety and Effects on Blood Pressure of Daily Dose 0.025 to 0.135 Milligram Per Kilogram of S90625 a Paediatric Formulation of Perindopril, in Hypertensive Children - 24 Months

Important dates

Study start
2003
Primary completion
2010
Study completion
2010
First posted
Sep 20, 2005
Registry last updated
Apr 12, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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