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Pelvis fracture recovery: can patients walk right after surgery?

NCT ID NCT07189156

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 26, 2026

Summary

This study looks at whether it's practical to run a larger trial comparing immediate weight bearing versus waiting 6-12 weeks after surgery for pelvis or acetabulum fractures. Researchers will enroll 200 adults from 7 medical centers and randomly assign them to either start walking right away or delay weight bearing. The main goal is to see if patients and surgeons are willing to participate, if patients follow instructions, and if follow-up is good.

What this could mean

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

Active substance
Immediate or delayed weight bearing as tolerated
What this could lead to
If successful, this study could show that a larger trial comparing immediate versus delayed weight bearing after pelvic surgery is possible, potentially leading to better recovery guidelines.
What could go wrong
This is a small feasibility study, not designed to prove which approach is better. Results may not change practice directly, and patient compliance or surgeon willingness could be low.

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 200 people

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

Expected to start

Oct 2025

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.

Ages

18 years and older

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. Adults 18 years old and above 2. Patients with surgically treated pelvis or acetabulum fractures Exclusion Criteria: 1. Presence of fractures to the ipsilateral or contralateral lower extremity that would preclude WBAT on the surgically repaired pelvis/acetabulum fracture 2. Presence of upper extremity injury that would limit weight bearing using an assistive device such as a walker or crutches 3. Severe injuries to other body systems that would prevent patient from being able to comply with weight bearing protocol 4. Presence of significant psychiatric or cognitive disorder or disability that would prevent patient from being able to comply with weight bearing protocol 5. Pre-injury non-ambulatory status 6. Suspected issues with follow-up 7. Language barriers precluding obtaining adequate informed consent

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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

    7 sites in 2 countries. 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

  • Arrowhead Regional Medical Center

    Colton, California, 92324, United States

  • Indiana University Health

    Indianapolis, Indiana, 46202, United States

  • Inova Medical Group

    Fairfax, Virginia, 22031, United States

  • R Adams Cowley Shock Trauma Center - University of Maryland

    Baltimore, Maryland, 21201, United States

  • University of Alabama Birmingham

    Birmingham, Alabama, 35233, United States

  • University of Mississippi Medical Center

    Jackson, Mississippi, 39216, United States

  • Vancouver General Hospital - University of British Columbia

    Vancouver, British Columbia, V5Z 1M9, Canada