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Smaller cuts, better recovery? study compares pelvic fracture surgeries

NCT ID NCT07534579

What the study statuses mean

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026

Summary

This study looks back at medical records of 60 adults who had surgery for severe pelvic fractures. It compares the standard open surgery (large cut) with a newer minimally invasive method (small cuts) to see which leads to better healing, fewer complications, and faster return to work. The goal is to help surgeons choose the best approach for each patient.

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 60 people

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

Expected to start

May 2026

An estimate. Start dates often move.

Expected to finish

Jun 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.

Who is studied

The study population consists of adult patients ($\\ge$ 18 years) treated at the Department of Orthopedic Surgery and Traumatology at Assiut University. Patients must have a confirmed diagnosis of a traumatic, unstable sacral fracture (including Denis Zones I-III with instability, spinopelvic dissociation, or AO/OTA Type C injuries). All included subjects were operated on using either open or minimally invasive lumbopelvic fixation between January 2016 and December 2024. Furthermore, participants must have adequate medical records with a minimum of 12 months of postoperative clinical follow-up.

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: * Adult patients aged 18 years or older at the time of injury and surgery. * Confirmed diagnosis of a traumatic, unstable sacral fracture, including: Denis Zone I, II, or III fractures with instability; Spinopelvic dissociation (U-type / H-type sacral fractures); AO/OTA Type C pelvic ring injuries involving the sacrum. * Operated on using lumbopelvic fixation (open or minimally invasive technique) within the study period (2016-2024). * Availability of adequate and complete medical records, including: Preoperative and postoperative imaging (X-ray and/or CT scan), and operative notes and surgical logs. * Minimum clinical follow-up of 12 months postoperatively. Exclusion Criteria: * Pathological fractures (e.g., fractures secondary to primary or metastatic malignancy, osteoporotic insufficiency fractures). * Patients managed conservatively or with alternative fixation strategies that do not include lumbopelvic instrumentation (e.g., isolated iliosacral screw fixation, anterior ring fixation alone). * Severe polytrauma resulting in in-hospital mortality prior to the minimum required follow-up period. * History of previous pelvic, sacral, or lumbosacral spine surgery prior to the index trauma. * Incomplete medical records or inadequate radiological follow-up data preventing accurate assessment of outcomes. * Patients with pre-existing neuromuscular disorders or spinal pathology that would confound neurological or functional outcome assessment. * Pregnant patients at the time of injury

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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How to take part

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  1. The official record

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