GPS for hip surgery: new navigation tool aims to improve fracture repair
NCT ID NCT04494672
First seen Jun 26, 2026 · Last updated Sep 09, 2026 · Updated 2 times
Summary
This trial tests whether a computer navigation system called ADAPT helps surgeons place screws more accurately during hip fracture repair. About 96 adults aged 50-85 with certain hip fractures will be randomly assigned to receive surgery with or without the navigation system. The main goal is to see if the system improves screw placement and reduces surgery time and radiation exposure.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- computer navigation system (ADAPT)
- What this could lead to
- If it works, this could make hip fracture surgery safer and faster, with fewer complications like screw misplacement.
- What could go wrong
- This is a small, early-stage trial with only 96 participants, so results may not apply to all patients. The navigation system may not improve outcomes enough to justify its use.
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
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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
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About 96 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2020
- Expected to finish
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Aug 2028
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.
- Ages
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50 to 85 years
- 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: * Patients undergoing unilateral primary intramedullary nailing at the Ospedale Regionale di Lugano. * Patients aged 50-85 years old. * Patients with a BMI \>18 and \<35. * Patients able to provide informed consent and follow all the study procedures as indicated by the protocol. * Radiological evidence of proximal fracture of the femur, AO classified as 31 A1.3, 31 A2.1, 31 A2.2, 31 A2.3, 31 A3.1, 31 A3.2, 31 A3.3. Exclusion Criteria: * Other clinically significant concomitant disease states (e.g. renal failure, major hepatic dysfunction, life-threatening cardiovascular disease, etc..). * Known or suspected non-compliance, drug or alcohol abuse. * Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant. * Previous enrolment into the current study. * Enrolment of the investigator, his/her family members, employees and other dependent persons.
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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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Christian Candrian
RECRUITINGLugano, 6900, Switzerland
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