Clinical trial Recruiting at 1 site Observational Ages 18 and up

Measuring muscle strength and size in people with inflammatory bowel disease.

Official title: Evaluation of Sarcopenia in Patients With Inflammatory Bowel Disease

Run by Sakarya University · NCT07441447 · Data updated 2026-11-12

This project will test whether ultrasound measurements of selected muscles, together with handgrip strength, can serve as a practical alternative to CT-based muscle measurements for adults with inflammatory bowel disease.

More Crohn Disease (CD) trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment100 (estimated)
SponsorSakarya University
Academic / other
Drugs / interventionsradiation
Locations1 site (Sakarya, Adapazarı)
StatusRecruiting
StartedNovember 10, 2025
Main results expectedNovember 10, 2026
Study endsDecember 2026
Registry record updatedMarch 2, 2026
Trial IDNCT07441447 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (≥18 years) with a confirmed diagnosis of IBD who can provide informed consent, undergo handgrip testing and muscle ultrasound, and have an abdominal CT performed within the previous six months are ideal candidates.

Probably not a fit

Patients with known neuromuscular disorders, major orthopedic limitations affecting strength testing, abdominal wall defects, pregnancy, or incomplete clinical or imaging data are unlikely to benefit from this protocol.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This prospective, single-center observational project enrolls adults with confirmed IBD to measure muscle strength and muscle mass using handgrip dynamometry and targeted muscle ultrasonography. Selected muscles (rectus femoris, vastus intermedius, gastrocnemius medialis, biceps brachii, rectus abdominis, and internal oblique) will be measured for thickness and cross-sectional area by ultrasound. For participants with an abdominal CT within the previous six months, L3 skeletal muscle cross-sectional area will be measured from archived images to compare with ultrasound results. The primary outcome is the correlation and agreement between ultrasound-based measures and CT-derived L3 muscle area.

Why it matters

Potential benefit: If successful, ultrasound could offer a fast, radiation-free, and more accessible way to monitor muscle mass in patients with IBD.

How similar studies have gone: Ultrasound has shown promising agreement with CT for muscle measurement in other patient groups, but validation specifically in IBD populations remains limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age ≥18 years
* Established diagnosis of inflammatory bowel disease (ICD-10: K50.\* Crohn's disease, K51.\* ulcerative colitis)
* Ability to provide written informed consent
* Ability to undergo ultrasonographic muscle assessment and handgrip strength testing
* Availability of an abdominal computed tomography (CT) scan performed within the previous 6 months

Exclusion Criteria:

* Known neuromuscular disorders or primary muscle diseases
* Major orthopedic conditions affecting muscle strength assessment
* Pregnancy
* Abdominal wall defects or conditions interfering with ultrasound assessment
* Incomplete clinical or imaging data
* Any condition preventing reliable ultrasound or handgrip measurement

Where it's running

  • Sakarya University Faculty of Medicine, Training and Research Hospital
    Sakarya, Adapazarı, Turkey (Türkiye)
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.