Blood loss after hip break may rob seniors of independence
NCT ID NCT03810092
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tracked 255 patients aged 75 and older who had surgery for a broken hip. Researchers wanted to see if low red blood cell counts (anemia) soon after surgery were linked to losing the ability to do daily tasks like dressing and bathing six months later. The goal is to better understand which patients might need extra help to stay independent.
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 it succeeds, this could help doctors identify which elderly patients need extra support after hip fracture surgery to maintain their independence.
- What could go wrong
- This is an observational study, not a treatment trial, so it cannot prove cause and effect. Results may not apply to all patients or settings.
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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255 people
The number who actually took part.
- Started
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May 2019
- Finished
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Apr 2023
- 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
This study is intended for patients over 75 years of age who have had a fracture of the upper extremity of the femur operated on.
- Ages
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75 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 ≥ 75 years * Patient operated on a fracture of the upper extremity of the femur * Patient, family or close relative who does not object to participation in the study * Patient affiliated to a social security system * Patient who can be monitored as part of the protocol Exclusion Criteria: * Refusal to participate in the study (patient, family or trusted relative) * Patient with support on the operated limb not authorized by the surgeon * Patient with an associated fracture (polytrauma, concomitant trauma to the upper limb...) * Patient with a pathologic fracture * Patient included in Category 1 interventional research (involving a drug or medical device) * Patient deprived of liberty * Patient not affiliated to a social security system
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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
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CH Cholet
Cholet, France
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CH La Rochelle
La Rochelle, France
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CH Saint Malo
St-Malo, France
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CHU Angers
Angers, France
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Centre Hospitalier Départemental Vendée
La Roche-sur-Yon, France
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