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2026-526044-12-00Not yet recruitingPhase 4

Efficacy and safety of pharmacological therapy of obesity in liver transplant candidates

Source: EU CTIS (euclinicaltrials.eu) · Last updated 18 Mar 2026

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Brief summary (registry, in English)

To evaluate the efficacy and safety of pharmacological obesity treatment (BMI ≥ 30) in liver transplant candidates.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
40 (estimated)
First submitted
9 Mar 2026
Start date
1 Jan 2027
Lead sponsor
Institute For Clinical And Experimental Medicine
Diseases
Obesity
EU CT number
2026-526044-12-00

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 40
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Combined liver-kidney transplantation.
  • Sarcopenia according to pre-transplant CT.

Other illness

  • Pregnancy (pre-enrollment assessment includes a pregnancy test; women of childbearing potential must agree to use highly effective contraception — hormonal or barrier methods, or abstinence; highly effective methods are defined as those with failure rate <1% per year with correct and consistent use).
  • History of acute or chronic pancreatitis.
  • Polycystic liver disease
  • Type 1 diabetes mellitus
  • Liver malignancy outside Milan criteria (Milan-out, Klatskin tumor, colorectal carcinoma metastases, NET metastases).
  • Unstable clinical condition or unplanned hospitalization due to significant deterioration or complication.

Other

  • Hepatic encephalopathy
  • Refractory ascites/hydrothorax (≥2 evacuation procedures in the last 2 months).
  • Spontaneous weight loss (≥5% in the past 6 months, not due to diuretic or evacuation treatment).
  • Inability to perform physical activity (walking 30 min/day).

Who the study is looking for

  • Liver transplant candidate undergoing pre-transplant evaluation (inpatient or outpatient) at the Department of Hepatogastroenterology, aged ≥18 years.
  • BMI ≥ 30, or BMI ≥ 33 in case of significant fluid retention (edema of lower extremities, ascites, hydrothorax; for large ascites/hydrothorax, BMI will be evaluated after evacuation puncture).
  • Clinically stable (patient is at home under outpatient follow-up or hospitalized on a standard ward without clinical or laboratory signs of significant deterioration or complications).
  • Signed informed consent.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Institute for Clinical and Experimental MedicinePragueCzechiaNot yet recruiting

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This page is information, not medical advice. Discuss any trial with your doctor.