Trials / Completed
CompletedNCT02184858
Dose Titration of Lisinopril in Children Aged 1 to 18 Years With Primary or Secondary Hypertension
Dose Titration Study to Test Efficacy and Safety of Lisinopril in Children Aged 1 to 18 Years With Primary or Secondary Hypertension.
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 13 (actual)
- Sponsor
- University Ghent · Academic / Other
- Sex
- All
- Age
- 1 Year – 18 Years
- Healthy volunteers
- Not accepted
Summary
This open label 4 month study will evaluate efficacy (blood pressure lowering effects) and safety of lisinopril in children 1-18y whose parents grant permission to participate. This dose titration study is being conducted to support the statement that personalized titration of lisinopril (based on blood pressure and renin-aldosterone ratio) can increase patient response.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | lisinopril, ACE-inhibitor | Lisinopril 0.1mg/kg/d, titration with + 0.1mg/kg/d. Max; daily dose: 0.4mg/kg. CAVE: dose reduction in case of renal impairment |
Timeline
- Start date
- 2014-06-25
- Primary completion
- 2017-05-08
- Completion
- 2018-09-17
- First posted
- 2014-07-09
- Last updated
- 2018-09-20
Locations
1 site across 1 country: Belgium
Source: ClinicalTrials.gov record NCT02184858. Inclusion in this directory is not an endorsement.