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Blood test clues may predict survival after hip surgery in seniors

NCT ID NCT07607886

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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

Summary

This study looks back at medical records of 233 older adults (65+) who had hip fracture surgery. Researchers want to see if certain blood test results, taken before and after surgery, can help predict who is at higher risk of dying within 30 days or needing a longer stay in the intensive care unit. The goal is to find simple, widely available markers that could help doctors better manage care for elderly hip fracture patients.

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 233 people

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

Started

Jan 2021

Expected to finish

Jun 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

Geriatric patients aged 65 years and older who underwent proximal femoral nailing (PFN) surgery for intertrochanteric femur fractures at a tertiary referral center were retrospectively evaluated. The study population consisted of patients with available perioperative laboratory data, 30-day mortality information, and intensive care unit follow-up records.

Ages

65 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: * Patients aged 65 years and older * Diagnosis of intertrochanteric femur fracture * Undergoing proximal femoral nailing (PFN) surgery * Availability of preoperative laboratory data * Availability of early postoperative laboratory measurements * Availability of 30-day mortality data * Availability of intensive care unit admission and ICU length of stay data * Complete electronic medical records Exclusion Criteria: * Patients with missing clinical or laboratory data * Pathological fractures * Multiple trauma patients * Revision surgeries * Presence of active infection or sepsis before surgery * Hematologic diseases that could affect inflammatory indices * Unavailable 30-day mortality or ICU data

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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

  • University of Health Sciences Gazi Yaşargil Training and Research Hospital

    Diyarbakır, Diyarbakır, Turkey (Türkiye)

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