Myokines as Potential Biomarkers and Drivers of Sarcopenia in Metabolic and Endocrine Diseases
SARC-ENDO
1 other identifier
observational
100
1 country
1
Brief Summary
Prospective, observational, single-center, study evaluating the prevalence of sarcopenia / sarcopenic obesity in individuals with metabolic and / or endocrine diseases, as well as the potential role of myokines as biomarkers or drivers of sarcopenia / sarcopenic obesity in this population. .
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Feb 2026
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 19, 2026
CompletedFirst Submitted
Initial submission to the registry
May 15, 2026
CompletedFirst Posted
Study publicly available on registry
July 14, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2056
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2056
July 14, 2026
May 1, 2026
30.9 years
May 15, 2026
July 10, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Prevalence of sarcopenia / sarcopenic obesity
From February 2026 to december 2056
Secondary Outcomes (4)
Myokines levels in serum or plasma
February 2026 to December 2056
Myokine expression
February 2026 to December 2056
Prevalence of MASLD
March 2026 to December 2056
Prevalence of MASH
March 2026 to December 2056
Interventions
Participants receive GLP-1 RA or GLP-1/GIP dual agonists as part of their standard care for overweight or obesity
Eligibility Criteria
People with metabolic or endocrine diseases
You may qualify if:
- Metabolic or endocrine disease
You may not qualify if:
- Known myopathy
- Systemic steroid use (\> 1 mg/kg hydrocortisone) or exogenous Cushing's syndrome
- Psychological, family, sociological or geographical conditions that could potentially limit compliance with the study protocol
- History of cancer within the five years prior to the study or Cushing's syndrome due to ACTH-secreting tumor
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Cliniques Universitaires Saint-Luc
Woluwe-Saint-Pierre - Sint-Pieters-Woluwe, 1150, Belgium
Biospecimen
Serum, plasma, muscle tissue
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 15, 2026
First Posted
July 14, 2026
Study Start
February 19, 2026
Primary Completion (Estimated)
December 31, 2056
Study Completion (Estimated)
December 31, 2056
Last Updated
July 14, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share