Bone density and weight linked to severe hip fractures in elderly women

NCT ID NCT07196982

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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.
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Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
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 Results may not be published yet.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

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Status unknown
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First seen Jun 27, 2026 ยท Last updated Jun 27, 2026

Summary

This study examined 49 older women with hip fractures to understand why some also break a supportive bone called the lateral wall. Researchers found that lower bone density and lower body weight were linked to these more complex fractures. The goal is to help doctors plan better surgeries and recommend bone health and fall prevention strategies.

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 better predict which elderly women are at risk for complex hip fractures, leading to improved surgical planning and preventive care.
What could go wrong
This is a small, retrospective study with only 49 participants, so findings may not apply to all populations. It identifies risk factors but does not test a treatment.

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

49 people

The number who actually took part.

Started

Jan 2023

Finished

Feb 2024

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 consisted of postmenopausal women admitted to the Department of Orthopedics at the Second Affiliated Hospital of Soochow University between January 2023 and February 2024 with a diagnosis of intertrochanteric femoral fracture. A total of 49 patients were included after applying eligibility criteria. Of these, 29 had isolated intertrochanteric fractures and 20 had intertrochanteric fractures with concomitant lateral wall involvement. All patients underwent surgical fixation with proximal femoral nail antirotation (PFNA), with or without additional lateral wall plate fixation, according to clinical indications.

Ages

65 to 85 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: Postmenopausal women diagnosed with intertrochanteric femoral fractures. History of low-energy trauma (e.g., fall from standing height). Treated surgically with proximal femoral nail antirotation (PFNA) device, with or without lateral wall plate fixation. Availability of complete demographic and clinical data (age, height, weight, bone mineral density, and bone turnover markers). Eligible for retrospective case-control analysis. Exclusion Criteria: High-energy trauma (e.g., motor vehicle accidents). Severe systemic comorbidities such as hepatic or renal failure, bone tumors, or endocrine disorders (e.g., hyperparathyroidism). Use of medications affecting bone metabolism within 6 months before surgery. Diagnosis of diabetes mellitus. History of chronic smoking or alcohol abuse. Inability to provide accurate anthropometric data (height and weight).

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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

  • The medical record system and imaging system of the Second Affiliated Hospital of Soochow University

    Suzhou, Jiangsu, 252000, China