Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
50 participants
INTERVENTIONAL
2024-05-01
2026-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
BASIC_SCIENCE
NONE
Study Groups
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Surgical patients
Patients undergoing surgery
Myosteatosis
Determination of myosteatosis by imaging
Non surgical patients
Patients not undergoing surgery
Myosteatosis
Determination of myosteatosis by imaging
Interventions
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Myosteatosis
Determination of myosteatosis by imaging
Eligibility Criteria
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Inclusion Criteria
* Treatment and estimated survival of more than 3 months
* Signed informed consent
* \> 18 years of age
Exclusion Criteria
* Cognitive disorders
* Psychiatric disorders
* Inability to communicate in French or English
18 Years
ALL
No
Sponsors
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Cliniques universitaires Saint-Luc- Université Catholique de Louvain
OTHER
Responsible Party
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Principal Investigators
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Yannick Deswysen, MD
Role: PRINCIPAL_INVESTIGATOR
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Locations
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Cliniques universitaires Saint-Luc
Brussels, , Belgium
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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TuMECA
Identifier Type: -
Identifier Source: org_study_id
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