Actively Recruiting
Sarcopenia in Cirrhosis and Chronic Inflammatory Bowel Disease: An Austrian Biobanking Study
Led by Medical University of Graz · Updated on 2024-10-09
1000
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are conducting a biobanking study in Austria to better understand sarcopenia, a condition marked by progressive loss of muscle mass, strength, and quality, especially common in older adults and patients with liver cirrhosis or chronic inflammatory bowel disease. The study aims to collect standardized clinical and biochemical data along with biosamples to explore new biomarkers and advanced clinical assessments. This nationwide effort hopes to expand to all tertiary liver care centers in Austria to enhance research capabilities. Participants will be categorized based on whether they meet the European Working Group on Sarcopenia in Older People (EWGSOP) criteria for sarcopenia or not. The study involves collecting routine clinical data, biochemical tests, and imaging scans like CT or MRI performed as part of standard care within two months of the study visit. The data and samples will be used to build a detailed registry and biobank for sarcopenia research. During the study, participants undergo assessments including muscle strength and function tests, imaging reviews, and biosample collection. Researchers will create an Austrian-wide sarcopenia register at enrollment and analyze clinical, biochemical, and imaging data. There is no investigational treatment given; instead, the focus is on collecting comprehensive information to improve diagnosis and understanding. Participation involves consenting adults who have recent imaging as part of their care and excludes those with severe cognitive impairment or advanced liver cancer. The study is expected to continue through 2035.
CONDITIONS
Brief Title
Austrian Biobanking Study for Sarcopenia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age over 18 years
- Ability to provide informed consent
- CT or MRI scan performed as part of routine care within 2 months before or after the study visit
You will not qualify if you...
- Hepatic encephalopathy greater than grade 2 or other cognitive disorders preventing informed consent
- Hepatocellular carcinoma stage BCLC C or D
- Any condition or circumstance that may affect the ability to participate as judged by the investigator
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - At enrollment
Participants undergo assessments including CT or MRI scans and clinical evaluations to diagnose sarcopenia status according to established criteria.
1 visit (in-person)
Duration - Up to 12 years
Participants are observed over time to collect data on sarcopenia progression and related health outcomes.
Trial Site Locations
Total: 1 location
1
Medical University of Graz
Graz, Austria, 8010
Actively Recruiting
Research Team
V
Vanessa Stadlbauer, MD
L
Lavra Celcer, MSc
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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