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1500 fracture patients tracked to unlock recovery secrets

NCT ID NCT04113044

Knowledge-focused Sponsor: AO Innovation Translation Center 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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study follows about 1500 adults with hip, shin, ankle, upper arm, or wrist fractures for up to one year. Researchers collect information on healing, patient-reported symptoms, and activity patterns using questionnaires and wearable sensors. The goal is to understand recovery trajectories and improve future fracture care.

What this could mean

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

What this could lead to
If successful, this study could help doctors better predict recovery and tailor treatments for common fractures.
What could go wrong
This is an observational study, not testing a new treatment. It may not lead to immediate changes in care.

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 1,500 people

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

Started

Feb 2021

Expected to finish

Dec 2026

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

All patients over 18 who have have suffered an isolated fracture of one of the following five bones: 1. proximal femur (hip); 2. tibial shaft (shin bone); 3. ankle; 4. proximal humerus (shoulder); and 5: distal radius ( wrist)

Ages

18 years and older

Sex

Anyone

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: * Age 18 years and older * Diagnosis of one of, isolated injury * Hip fracture * Tibial shaft fracture (with and without associated fibular fracture) * Ankle/pilon fracture * Proximal humerus fracture * Distal radius fracture * English, German, or Spanish speaking * Informed consent obtained, i.e.: * Ability to understand the content of the patient information/ICF * Willingness and ability to participate in the clinical investigation according to the Clinical Investigation Plan (CIP) * Signed and dated EC/IRB approved written informed consent Exclusion Criteria: * More than 21 days from day of injury to day of surgery / day of nonoperative treatment decision * Patients with multiple fractures * Pathological fractures due to cancer * Recent history of substance abuse (i.e. recreational drugs, alcohol) that would preclude reliable assessment * Pregnancy or women planning to conceive within the study period * Patients who are not able to provide independent written informed consent unless defined and IRB/IEC-approved procedures for consenting such vulnerable patients are in place * Prisoners * Participation in any other medical device or medicinal product study within the previous month that could influence the results of the present study * Patients unable to likely achieve anticipated Follow-up (FU)

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Conditions

The condition(s) this trial relates to.

Ankle Fractures hip fracture humerus fracture radius fracture Shoulder Fractures tibia fracture Wrist Fractures

As listed by the trial registrant

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

Ankle fractures Distal radius fracture Hip fractures Humeral fracture, proximal Tibial fractures

Contacts and locations

Locations

  • Abteilung für Unfall- und Wiederherstellungschirurgie BG Klinik Tübingen

    Tübingen, 72076, Germany

  • Barts Health NHS Trust

    London, E14DG, United Kingdom

  • Cedars-Sinai Department of Orthopaedics

    Los Angeles, California, 90048, United States

  • Centrum für Muskuloskeletale Chirurgie (CMSC) Charite - Universitätsmedizin Berlin

    Berlin, 13353, Germany

  • Fundación Santa Fe de Bogotá

    Bogotá, 110121, Colombia

  • Institut für Biomechanik Berufsgenossenschaftliche Unfallklinik Murnau

    Murnau am Staffelsee, 82418, Germany

  • Isala Clinics

    Zwolle, 8000, Netherlands

  • Massachusetts General Hospital Harvard Orthopaedic Trauma Initiative

    Boston, Massachusetts, 02114, United States

  • Oxford University Hospitals NHS Foundation Trust

    Oxford, OX39DU, United Kingdom

  • Saarland University Hospital Department of Trauma, Hand and Reconstructive Surgery

    Homburg, 66421, Germany

  • The Value Institute / Department of Surgery and Peri-operative Care. Dell Medical School, University of Texas at Austin

    Austin, Texas, 78712, United States

  • Univ.-Klinik für Orthopädie und Traumatologie

    Innsbruck, 6020, Austria

  • University Hospital Freiburg

    Freiburg im Breisgau, 79106, Germany

  • University Medical Center Groningen

    Groningen, 9700, Netherlands

  • University of Miami, Jackson Memorial Hospital Ryder Trauma Center

    Miami, Florida, 33136, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.