ClinicalTrials.gg
Active, not recruitingNCT07049289REMOTE-ControlUpdated Jul 3, 2025

Telemonitoring in Arterial Hypertension

An interventional study of Telemonitoring in Arterial Hypertension and Uncontrolled Hypertension, sponsored by Heart Center Leipzig - University Hospital. Active, not recruiting at 1 site in Germany. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-07-03.

Sponsored by Heart Center Leipzig - University Hospital · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 1 year 6 months after the study started (first participant enrolled Dec 2023, registered Jun 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 282 studies in Hypertension with a site in Germany — 30 open to participants now, 46 under way, 11 of them phase 3. Hypertension · Germany.

Enrollment
202nd of 250
60 · median 200
Started
2023
with 7 others
No phase
67 of 282
16 open now
Primary completion
2025-03
later than 11 of 45 live
Registered
273rd of 282
by date

Among the 282 studies in Hypertension with a site in Germany, this one is the 202nd largest by enrollment of the 250 interventional ones that give a count, is one of 8 that started in 2023, is one of 67 with no phase, reaches primary completion later than 11 of the 45 other live ones, and was the 273rd registered.

Hypertension

6,114 studies on the registry are indexed under Hypertension; 912 are open to participants now.

This study's enrollment of 60 is below the median of 100 across 4,575 interventional studies indexed under Hypertension.

Browse Hypertension studies →

Open to participants now

30 of the 282 studies in Hypertension with a site in Germany are open now.

All 30 open studies →

A study can be open while its sites in Germany have not opened yet or have stopped. Only those recruiting at a site in Germany →

Who these studies take

Of the 564 Hypertension studies recruiting now, 266 (47%) set no upper age limit and 200 (35%) stop at 75 or younger; 40 take children under 18; 138 take healthy volunteers.

This study: 18 Years and older · all sexes · no healthy volunteers.

The full table on the hub →
Was this useful?
Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 282 studies in Hypertension with a site in Germany, or all of them as a file.
02

Study summary

Prospective, randomized trial to assess the effects of a telemedical approach of antihypertensive treatment in comparison with standard care.

Total patient number: 60 patients.

  • Intervention group: biweekly telephone calls
  • Control group: standard of care
03

Conditions studied

  • Arterial Hypertension
  • Uncontrolled Hypertension

Browse trials for

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Confirmed arterial hypertension with systolic or diastolic blood pressure >140/90 mmHg in standardized office blood pressure measurement
  2. Treatment with 1 to ≤4 antihypertensive drug classes
  3. Age >18 years
  4. Written

Exclusion criteria

Exclusion Criteria:

  1. Pregnancy
  2. Participation in other randomized trials
  3. Patients under legal supervision or guardianship
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
60 participants (actual)

Study arms

  • No intervention
    Control

    Patients with arterial hypertension randomized to control arm with standard of care without additional interference through study team

  • Experimental
    Telemedical treatment

    Patients randomized to intervention group will receive biweeky telephone calls and adaption of antiyhpertensive medication if needed

    Other: Telemonitoring

Interventions

  • OtherTelemonitoring

    Patients randomized to intervention group will receive biweeky telephone calls and adaption of antiyhpertensive medication if needed

    Also known as: telemedicine

06

What researchers measure

Primary outcomes

  1. Time in blood pressure target range from randomization through 6 months

    Time in target range of each blood pressure measurement in first 6 months between control and intervention group

    Time frame: 6 months

Secondary outcomes

  1. Time in target range months 6 to 12

    Time in target range of each blood pressure measurement between control and intervention group from months 7 to 12

    Time frame: 6 months (7-12 months)

  2. Medication adherence as assessed by blood/urine sampling after 6 and 12 months

    Medication adherence as assessed by blood/urine sampling after 6 and 12 months

    Time frame: 0, 6 and 12 months

07

Study locations

1 site
  • Heart Centre Leipzig
    Leipzig, Germany
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Dec 2023 to primary completion in Mar 2025, 14 months.

Of 1,403 non-industry interventional studies with no phase under Hypertension, half reached primary completion within 23 months of starting (the median), counting those still running; a quarter within 10 and three quarters within 41. This study's 14 months is below that.

Counting every sponsor, half of 1,498 studies reached it within 23 months; a quarter within 10 and three quarters within 41.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 25, 2025
First posted
Jul 3, 2025
StartActual
Dec 13, 2023
Primary completionActual
Mar 9, 2025
CompletionEst.
Sep 9, 2025
Last update
Jul 3, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 3, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07049289
Lead sponsor
Heart Center Leipzig - University Hospital
Responsible party
Sponsor
First posted
Jul 3, 2025
Start date
Dec 13, 2023
Primary completion
Mar 9, 2025
Completion
Sep 9, 2025 (estimated)
Last update
Jul 3, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Jun 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion