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2024-519637-32-00Not yet recruitingPhase 2

Effect of Cannabidiol on Muscle Mass and Mitochondrial Function in Head and Neck Cancer

PANACEA : Effect of PrehAbilitation by NutritionAl supplementation with Cannabidiol on skeletal muscle mass and mitochondrial function in hEad and neck cAncer : a proof of concept controlled randomized trial

Source: EU CTIS (euclinicaltrials.eu) · Last updated 30 Jan 2026

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Brief summary (registry, in English)

Improvement of muscle health assessed by muscle mitochondrial activity perioperatively by adding cannabidiol (CBD) to nutritional supplementation in head and neck cancer

Status (registry)
Not yet recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
30 (estimated)
First submitted
27 May 2025
Start date
1 Jun 2025
Lead sponsor
University Hospital Of Clermont-Ferrand
EU CT number
2024-519637-32-00

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 30
  • 2 sites 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

  • Addiction to other drugs or cannabis
  • Malnutrition prior to the onset of head and neck cancer

Other illness

  • History of severe heart failure, severe respiratory failure, severe renal failure, severe chronic obstructive pulmonary disease, uncontrolled insulin-dependent diabetes or uncontrolled coronary artery disease
  • History of chemotherapy or radiotherapy for head and neck cancer
  • History of epilepsy

Age

  • Age <18 years

Other

  • Pregnant and breastfeeding women
  • Persons under curatorship, guardianship, protection of justice or deprived of liberty
  • Morbid obesity
  • Absence of nutritional risk (grade 1) or severe nutritional risk requiring urgent renutrition (grade 4) during the nutritional assessment

Who the study is looking for

  • Squamous cell carcinoma of the head and neck (oral cavity, oropharynx, hypopharynx, larynx or prevalent lymphadenopathy) or high probability of squamous cell carcinoma of the head and neck according to the judgment of the investigator (without histological confirmation)
  • Stage 2 or 3 nutritional risk according to the classification specific to this study (light to moderate nutritional risk)
  • Consent to participate in the study
  • For women of childbearing age: absence of current pregnancy and effective contraceptive method for the duration of treatment with CBD and up to 7 days after the end of treatment
  • To have of a means of communication (mobile phone) to monitor tolerance and appetite while taking CBD

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

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (2)

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

SiteCityCountrySite status
University Hospital Of Clermont-FerrandClermont-FerrandFranceNot yet recruiting
Chu Gabriel MontpiedClermont-FerrandFranceNot yet recruiting

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