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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03209154
Other study ID # 2017/6534
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date November 1, 2017
Est. completion date April 30, 2025

Study information

Verified date November 2023
Source Oslo University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to investigate and explore the most important aspects of drug-adherence in the treatment of hypertension in order to improve treatment and blood pressure control, implying that new knowledge will reduce morbidity and mortality.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 1000
Est. completion date April 30, 2025
Est. primary completion date December 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Signed informed consent - Uncontrolled hypertension - A stable medication regimen for at least 4 weeks of = 2 antihypertensive agents - No planned changes in antihypertensive drugs Exclusion Criteria: - Withdrawal of consent - 24-h systolic ambulatory blood pressure >/= 170 mmHg - Patients with inadequate Norwegian language skills - Positive pregnancy test - Known alcohol or drug abuse - estimated glomerular filtration rate <30 mL/min/1.73m2 - Albumin/creatinin ratio >300 mg/mmol - Any reason why, in the opinion of the investigator, the patient should not participate

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Therapeutic drug monitoring
Therapeutic drug monitoring will be performed.
Device:
Home blood pressure monitoring
Patients will perform home blood pressure monitoring at home.

Locations

Country Name City State
Norway Oslo University Hospital Oslo

Sponsors (5)

Lead Sponsor Collaborator
Oslo University Hospital Haukeland University Hospital, St. Olavs Hospital, University Hospital of North Norway, University of Oslo

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary Blood pressure control Change in systolic daytime ambulatory blood pressure. 3 months after baseline
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