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Effects of Temporary Inhibition of the Renin-Angiotensin System on future blood pressure and hypertensive organ damage in young prehypertensive adults * TIResiAS

Effects of Temporary Inhibition of the Renin-Angiotensin System on future blood pressure and hypertensive organ damage in young prehypertensive adults * TIResiAS - Temporary Inhibition of the Renin Angiotensin System - TIResiAS study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON30810
Enrollment
300
Registered
2007-02-01
Start date
2007-01-01
Completion date
Unknown
Last updated
2024-06-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

elevated blood pressure hypertension

Interventions

Individuals are randomized to receive either lisinopril 10mg daily for three weeks followed by lisinopril 20mg daily or matched placebo for a period of one year. This is followed by two years of reg

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Included are persons aged 18-40 years with an average blood pressure of 130-139 systolic/below 90 mmHg diastolic and/or below 130 systolic/ 85-89 mmHg diastolic on 3 separate office visits with an interval of one week as measured by an automated blood pressure device (Omron M4).

Exclusion criteria

Exclusion criteria: Excluded are persons with any (chronic) disease requiring medication or specialist treatment, patients with 3 or more risk factors according to current ESH guidelines, an elevated baseline serum glucose or elevated serum creatinine and females with a wish to become pregnant in the treatment period.

Design outcomes

Primary

MeasureTime frame
Blood pressure 2 years after cessation of active treatment as evidenced by differences in 24 hour ambulatory blood pressure measurements.

Secondary

MeasureTime frame
Differences in left ventricular mass and microalbuminuria 2 years after active treatment.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)