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Cuff trick may speed ankle surgery recovery

NCT ID NCT07451210

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests whether using a blood flow restriction (BFR) cuff during physical therapy helps people recover better after ankle ligament reconstruction surgery. About 105 adults will be split into two groups: one gets standard therapy, the other adds BFR. Researchers will measure muscle loss, ankle function, pain, and heart health over at least 6 weeks.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 105 people

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

Expected to start

Mar 2026

An estimate. Start dates often move.

Expected to finish

Dec 2027

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.

Ages

18 to 65 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: 1. Age 18-65 years. 2. Post ankle ligament reconstruction surgery (medial or lateral, with or without ankle scope). 3. Capability of paying for physical therapy or having insurance coverage for at least 6 weeks of therapy. Exclusion Criteria: 1. Major cardiac or connective tissue disorders (e.g., Ehlers-Danlos syndrome, Marfan syndrome). 2. Autoimmune disorders. 3. History of stroke or deep vein thrombosis (DVT). 4. Bleeding or coagulation disorders. 5. Congenital or developmental musculoskeletal disorders (e.g., cerebral palsy, Parkinson's disease). 6. Pregnancy (current or planning to become pregnant in the next 4 months) 7. Malignancy (cancer). 8. Professional athletes. 9. Workers compensation insurance status as worker's compensation often does not cover the necessary duration of physical therapy (minimum of 4 weeks). 10. Be currently enrolled or have been enrolled in another interventional clinical research study within the past 30 days (at time of consent); or 11. Be deemed unsuitable for inclusion in the study at the discretion of the Investigators 12. Cognitively not able to consent or participate in research (dementia; severe developmental delay; language/communication limitations; brain injury; etc.)

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

How to take part

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

  1. The places running it

    2 sites. 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

  • Northstar Surgery Center

    ACTIVE_NOT_RECRUITING

    Lubbock, Texas, 79416, United States

  • Physical Therapy Today (PTT)

    ACTIVE_NOT_RECRUITING

    Lubbock, Texas, 79407, United States

  • Texas Tech University Health Sciences Center

    RECRUITING

    Lubbock, Texas, 79430, United States

  • The Center for Orthopedic Surgery

    RECRUITING

    Lubbock, Texas, 79416, United States

  • University Medical Center

    ACTIVE_NOT_RECRUITING

    Lubbock, Texas, 79415, United States

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