Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
NA
60 participants
INTERVENTIONAL
2023-12-13
2025-09-09
Brief Summary
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Total patient number: 60 patients.
* Intervention group: biweekly telephone calls
* Control group: standard of care
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Control
Patients with arterial hypertension randomized to control arm with standard of care without additional interference through study team
No interventions assigned to this group
Telemedical treatment
Patients randomized to intervention group will receive biweeky telephone calls and adaption of antiyhpertensive medication if needed
Telemonitoring
Patients randomized to intervention group will receive biweeky telephone calls and adaption of antiyhpertensive medication if needed
Interventions
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Telemonitoring
Patients randomized to intervention group will receive biweeky telephone calls and adaption of antiyhpertensive medication if needed
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. Treatment with 1 to ≤4 antihypertensive drug classes
3. Age \>18 years
4. Written informed consent
Exclusion Criteria
2. Participation in other randomized trials
3. Patients under legal supervision or guardianship
18 Years
ALL
No
Sponsors
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Heart Center Leipzig - University Hospital
OTHER
Responsible Party
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Locations
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Heart Centre Leipzig
Leipzig, , Germany
Countries
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Other Identifiers
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REMOTE-Control-HTN
Identifier Type: -
Identifier Source: org_study_id
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