Could a simple ultrasound and nutrition score forecast hip fracture recovery?
NCT ID NCT07751692
First seen Aug 07, 2026 · Last updated Aug 07, 2026
Summary
This study looks at whether nutritional risk and muscle thickness can help predict recovery in adults aged 65 and older after hip fracture surgery. Researchers will measure nutritional status using a standard score and check muscle thickness in the thigh with a quick, painless ultrasound before surgery. They will then track hospital stay length, infections, and survival at 30 and 90 days after surgery to see if these simple measures are linked to better or worse outcomes.
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 could help doctors identify older patients at higher risk of complications after hip fracture surgery, allowing for earlier support and better recovery planning.
- What could go wrong
- This is an observational study, so it cannot prove cause and effect. The results may not apply to all patients, and the measures used may not fully capture recovery outcomes.
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
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About 120 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2027
An estimate. End dates often move.
- Lead sponsor
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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 will consist of consecutive patients aged 65 years or older who are admitted to Fatih Sultan Mehmet Training and Research Hospital with a hip fracture and are scheduled to undergo surgical treatment. Eligible participants of both sexes will be enrolled after informed consent is obtained. Participants will receive routine perioperative clinical care without any treatment allocation by the study.
- Ages
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65 years and older
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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 65 years or older * Scheduled to undergo surgical treatment for hip fracture * Provision of informed consent by the participant or, when applicable, a legally authorized representative Exclusion Criteria: * Pathological fracture or fracture related to malignancy * Advanced neuromuscular disease * Active infection * Planned revision surgery * Lower limb amputation or severe deformity preventing rectus femoris muscle thickness measurement * Inability to obtain informed consent from the participant or a legally authorized representative
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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
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University of Health Sciences, Fatih Sultan Mehmet Training and Research Hospital
Istanbul, 34000, Turkey (Türkiye)
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