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Which hip surgery route is best? new study aims to find out

NCT ID NCT04900506

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 compares two surgical techniques (posterior SPAIRE and anterior approach) for treating broken hips in people aged 70–90. Researchers will measure recovery, muscle damage, and bone density changes in 210 participants. The goal is to see if one approach leads to better outcomes, helping surgeons choose the best method for each patient.

What this could mean

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

Active substance
surgical procedure (posterior SPAIRE approach vs. anterior approach)
What this could lead to
If one approach proves better, it could guide surgeons to choose the method that leads to faster recovery and fewer complications for hip fracture patients.
What could go wrong
This is a relatively small, single-center study, and results may not apply to all hospitals or patient groups. The study is also observational in nature, so it cannot prove cause and effect.

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 210 people

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

Started

Jan 2022

Expected to finish

Sep 2026

An estimate. End dates often move.

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

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

Ages

70 to 90 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: * Patients between 70 and 90 years of age * Displaced FNF * Ability to walk with or without a walking aid prior to falling * Patients having Sorlandet Hospital as primary service provider for orthopaedic trauma * Provision of informed consent by patient or proxy * Low energy fracture (fall from standing height, no other major trauma) Exclusion Criteria: * Dementia * Fractures in pathologic bone * Patients not suited for HA (i.e., inflammatory arthritis, severe osteoarthritis) * Associated major injuries of the lower extremity ( i.e., ipsilateral or contralateral fractures of the foot, ankle, tibia, fibula or femur) * Retained hardware around the affected hip that will interfere with arthroplasty * Sepsis or local infection

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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.

Contacts and locations

Locations

  • Sorlandet Hospital

    Arendal, Norway

  • Sorlandet hospital

    Kristiansand, Norway

More trials for these conditions

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