New ultrasound test could spot muscle loss in seniors and cancer patients
NCT ID NCT01484821
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a new ultrasound technique (ARFI) to measure muscle stiffness in 65 volunteers: young adults (18-30), healthy older adults (70+), and older adults undergoing cancer treatment. The goal was to see if this method could help screen for sarcopenia (age-related muscle loss) better than current tests. Participants had physical exams, nutrition assessments, and muscle stiffness measurements at one or two visits over six months.
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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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65 people
The number who actually took part.
- Start date
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Nov 2011
- Finished
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Oct 2014
- 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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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Men or women 18 years old or more, * Able to understand the protocol and to give their written consent, * Health insurance. Specific inclusion criteria: * Group A: volunteers 18 to 30 yrs; without any pathology, * Group B: volunteers ≥ 70 yrs; without any pathology, * Group C: Performance status (ECOG) \< 4; patients included in CAPADOGE study presenting curative cares for cancer by chemotherapy and/ or surgery and/or hormonotherapy and/or radiotherapy. Exclusion Criteria: * Intense activity in 7 preceding days, * Functional dependency, * under a legal protection. Specific non-inclusion criteria: * Groups A \& B: serious chronic disease, * Group C: Palliative care.
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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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CHU Bordeaux - Hôpital Saint André
Bordeaux, 33000, France
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CHU de Bordeaux - Hôpital Haut-Lévêque
Pessac, 33600, France
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Other studies related to the condition(s) this trial covers.
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