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CompletedNCT07890129Updated Oct 22, 2026

Stopping Blood Pressure Medications Without Tapering in Long-Term Care

An interventional study of Deprescribing antihypertensives without a taper in Hypertension (HTN), sponsored by University of Alberta. Completed at 2 sites in Canada. Open to participants aged 80 Years and older. Per ClinicalTrials.gov, last updated 2026-10-22.

Sponsored by University of Alberta · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 1 year 4 months after the study started (first participant enrolled Jun 2025, registered Oct 2026).
Updated Oct 22, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
11
Allocation
Not applicable
Ages
80 Years and older
Sex
All
01

Study summary

Blood pressure medications may provide limited benefit and cause side effects in frail older adults. It is unclear how best to stop these medications. Guidelines often recommend gradually reducing the dose, but this process can be time-consuming. This study examined the feasibility of stopping blood pressure medications without gradually reducing the dose in long-term care residents with low blood pressure. Eligible residents had their medication stopped and were monitored for four weeks.

02

Conditions studied

  • Hypertension (HTN)

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Keywords

  • Taper
  • Deprescribing
  • Antihypertensives
  • Long-term Care
  • Frail
03

In context

Hypertension

6,834 studies on the registry are indexed under Hypertension; 971 are open to participants now.

This study's enrollment of 11 is below the median of 90 across 5,095 interventional studies indexed under Hypertension.

Browse Hypertension studies →

Lead sponsor

University of Alberta is the lead sponsor of 819 studies on the registry; 166 are open to participants now.

Of its 5 completed or terminated interventional studies of FDA-regulated products, 3 (60%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
80 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

  • Taking at least 1 daily antihypertensive medication
  • Average systolic blood pressure \< 130 mmHg

Exclusion criteria

Exclusion Criteria:

  • Diagnosis of congestive heart failure
  • Use of antihypertensives for indications other than hypertension
  • Hospitalization at the time of selection of participants
  • Physician or participant/substitute decision maker opt out
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
11 participants (actual)

Study arms

  • Experimental
    Antihypertensive Discontinuation Without Tapering

    Eligible long-term care residents had one blood pressure medication discontinued without gradually reducing the dose.

    Other: Deprescribing antihypertensives without a taper

Interventions

  • OtherDeprescribing antihypertensives without a taper

    Discontinuation of one antihypertensive medication without gradually reducing the dose.

06

What researchers measure

Primary outcomes

  1. Successful Antihypertensive Deprescribing

    Proportion of participants who discontinued one antihypertensive medication without tapering and remained off that medication for four weeks.

    Time frame: In the four weeks after medication discontinuation

Secondary outcomes

  1. Change in Systolic and Diastolic Blood Pressure

    Change in systolic and diastolic blood pressure from baseline to the end of the four-week follow-up period.

    Time frame: Baseline and four weeks after medication discontinuation

  2. Change in As-Needed Medication Use

    Change in the monthly number of as-needed medication administrations before and after stopping antihypertensive medication

    Time frame: Three months before and four weeks after medication discontinuation

  3. Change in Number of Falls

    Change in the number of falls before and after stopping antihypertensive medication

    Time frame: Six months before and four weeks after medication discontinuation

  4. Change in Meal Intake

    Change in the percentage of meals consumed before and after stopping antihypertensive medication, assessed using categories of 0-25%, 26-50%, 51-75%, and over 75%

    Time frame: Four weeks before and four weeks after medication discontinuation

07

Study locations

2 sites
  • Carewest Colonel Belcher
    Calgary, Alberta T3B 5Y8, Canada
  • Benevolence Care Centre
    Edmonton, Alberta T5P 3S7, Canada
08

Timeline

1 registry update 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 Jun 2025 to primary completion in Nov 2025, 5 months.

Of 1,339 non-industry interventional studies with no phase under Hypertension, half reached primary completion within 22 months of starting (the median), counting those still running; a quarter within 9 and three quarters within 42. This study's 5 months is below that.

Counting every sponsor, half of 1,433 studies reached it within 23 months; a quarter within 9 and three quarters within 43.

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

Registered
Oct 18, 2026
First posted
Oct 22, 2026
StartActual
Jun 1, 2025
Primary completionActual
Nov 30, 2025
CompletionActual
Nov 30, 2025
Last update
Oct 22, 2026
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.
Registered
First appeared on the registry. No changes since
Oct 22, 2026
Show all 1 update
  1. Oct 22, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07890129
Responsible party
Sponsor
First posted
Oct 22, 2026
Start date
Jun 1, 2025
Primary completion
Nov 30, 2025
Completion
Nov 30, 2025
Last update
Oct 22, 2026

Oversight

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

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This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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