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Taking people in FranceNo phase

Studies how one exercise session affects liver-related proteins in people with liver cancer

Tests a single endurance exercise session in adults with liver cancer.

Plain-language title generated from the registry record
Registry title: Effect of Acute Endurance Exercise on the Production of FGF21 and Follistatin in Patients With Hepatocellular Carcinoma

Key facts

Where
Clermont-Ferrand, FranceSee the 2 sites

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults aged 18 to 80 with liver cancer (hepatocellular carcinoma) that developed on cirrhosis. They will do one 30-minute bike session with blood tests.

Age
18 to 80 years
Sex
All sexes
Disease stage
Hepatocellular carcinoma on cirrhosis, planned for immunotherapy or chemoembolization. Child-Pugh score A or B7. WHO score of 2 or less.
Earlier treatment
No surgery in the 30 days before joining. No liver transplant.
Biomarker or test result
Cirrhosis shown by a liver elasticity measurement above 15kPa or a past cirrhosis decompensation.

Main reasons for not taking part

  • Hepatic encephalopathy grade II or higher
  • Bone metastasis
  • Muscle injury in the last 3 months
  • Pregnant or breast-feeding women
  • Another clinical trial in the last 10 days

Read by machine on 12 November 2026.

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 80 years old?

Source: NCT07189624, who can take part

Where in France

  • CHU de Clermont-FerrandClermont-Ferrand, FranceContact: lise LaclautreTaking people
  • Chu Estaing Medecine Digestive Et HepatobiliaireClermont-Ferrand, FranceContact: ARMANDO ABERGELNot yet recruiting

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
University Hospital, Clermont-Ferrand
Trial code
NCT07189624
Record updated
9 November 2026
Original description
The main purpose of the study is to characterize the production of hepatokines (FGF21 and Follistatin) in response to a submaximal exercise on an ergocycle, in patients with hepatocellular carcinoma. The effect of exercise on hepatokines and metabolites production in liver cancer patients is not known. Studying this production could help to provide relevant recommendations for training programming in these patients.Read full original descriptionShow less

Effect of Acute Endurance Exercise on the Production of FGF21 and Follistatin in Patients With Hepatocellular Carcinoma

The main purpose of the study is to characterize the production of hepatokines (FGF21 and Follistatin) in response to a submaximal exercise on an ergocycle, in patients with hepatocellular carcinoma. The effect of exercise on hepatokines and metabolites production in liver cancer patients is not known. Studying this production could help to provide relevant recommendations for training programming in these patients.

Inclusion: Hepatocellular carcinoma developed on cirrhosis; Cirrhosis of any etiology, defined by a liver elasticity measurement >15kPa or a history of cirrhosis decompensation; Hepatocellular carcinoma with indication for treatment by immunotherapy or chemoembolization; Child-Pugh scores A and B7; WHO score ≤ 2; Affiliation to french national social security system.

Exclusion: Surgery performed within 30 days prior to inclusion visit; Liver transplant; Hepatic encephalopathy grade II or higher; Bone metastasis; Muscle injury within 3 months of inclusion; Pregnant or breast-feeding women; Patients under legal protection (guardianship, curatorship, safeguard of justice); Participation in another clinical trial within 10 days of inclusion.

ClinicalTrials.gov NCT07189624