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New handheld device lets surgery patients check vitals at home

NCT ID NCT07231653

Knowledge-focused Sponsor: University of Alberta Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Aug 18, 2026 · Updated 2 times

Summary

This study tests a small, handheld device called the Wellvii VitalDetect that lets patients check their blood pressure, pulse, and temperature at home after surgery. About 69 adults will use the device twice daily for two weeks and compare results with clinic measurements. The goal is to see if the device is accurate and easy enough for patients to use on their own.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Wellvii VitalDetect (handheld vital sign monitor)
What this could lead to
If successful, this could show that patients can reliably monitor their own vital signs at home after surgery, potentially reducing hospital visits.
What could go wrong
This is a small, early-stage study with only 69 participants. The device may not be as accurate as clinic measurements, and results may not apply to all patients.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 69 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jan 2027

An estimate. Start dates often move.

Expected to finish

Dec 2028

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Patients undergoing surgical procedures, including day surgery procedures and those procedures requiring a hospital stay

Ages

18 to 80 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Clinically stable patients requiring routine postoperative monitoring in the absence of any acute illness following surgery. * Able to use a smartphone or tablet for the monitoring system. Exclusion Criteria: * Severe cognitive impairment or conditions that may interfere with the use of home monitoring devices. * Currently participation in other clinical trials involving vital sign monitoring. * Unable to provide informed consent.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Patient monitoring Postoperative period

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Mackenzie Health Science Centre

    Edmonton, Alberta, T6G 2B7, Canada

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