Skip to content

Resistente HYpertensie: MEten voor Resultaat op Controle Tensie

Resistant HYpertension: MEasure to Reach Targets

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON26643
Enrollment
310
Registered
2017-12-27
Start date
2018-07-01
Completion date
Unknown
Last updated
2024-06-11

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

Conditions

Resistant hypertension, therapieresistente hypertensie

Interventions

Feedback of actual drug levels measured in a dried blood spot (DBS) obtained by a finger prick combined with supported problem solving: firstly, barriers to adherence will be discussed and suggestions

Sponsors

Erasmus Medical Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - Resistant hypertension: office blood pressure > 140/90 mmHg and 24h ABPM (ambulatory blood pressure measurement) daytime blood pressure > 135/85 mmHg despite a medication regimen of antihypertensive drugs from at least three classes including a diuretic. - Use of at least two drugs for which DBS-analysis is available (enalapril, perindopril, losartan, valsartan, hydrochlorothiazide, spironolactone, amlodipine and nifedipine. - Age 18 years and older - Providing informed consent after reading patient information

Exclusion criteria

Exclusion criteria: - Not providing informed consent or not capable of giving informed consent - Kidney transplantation - End-stage renal disease (eGFR<15 ml/min) „h - Insufficient understanding of Dutch or Turkish language - Secondary forms of hypertension (to be excluded according to local guidelines) except cases when a secondary form of hypertension has been established or is likely but chosen treatment is drug therapy (for instance primary hyperaldosteronism, renovascular hypertension).

Design outcomes

Primary

MeasureTime frame
- Determine whether measuring drug levels combined with personalized feedback leads to a decrease in resistant hypertension after 12 months of follow-up.

Secondary

MeasureTime frame
- determine percentage of assumed resistant hypertension at baseline due to non-adherence - Determine the percentage of patients with partial or non-adherence at baseline who are adherent after 12 months of follow-up - Determine whether the number of required antihypertensive drugs is lower in patients who receive feedback on drug levels than in patients who do not. - cost-utility of the intervention versus usual care in resistant hypertention - The number of patients fulfilling the definition of resistant hypertension after 3 and 6 months

Contacts

Public ContactJorie Versmissen
j.versmissen@erasmusmc.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)