Evaluation of the Impact of Taking American Ginseng for 8 Weeks on Fatigue in Patients Treated for Localized Breast or Gynecological Cancer

Last updated: September 30, 2024
Sponsor: Centre Francois Baclesse
Overall Status: Active - Recruiting

Phase

N/A

Condition

Pain (Pediatric)

Breast Cancer

Cancer

Treatment

PLACEBO

QISENG

Clinical Study ID

NCT05241405
2021-A01550-41
  • Ages > 18
  • Female

Study Summary

This is a multicenter randomized trial in breast cancer patients reporting cancer-related fatigue to evaluate the efficacy and safety of Qiseng® based on extract of American ginseng combined with vitamin C from extract of Camu Camu berries

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients with localized breast or gynecological cancer treated as curative adjuvantand/or neoadjuvant chemotherapy and/or adjuvant radiotherapy. These treatments musthave been completed within 6 months of inclusion.

  • Patient reporting a chronic, stable fatigue state at investigator assessment,defined as a fatigue score ≥ 4 on the visual analog scale rated up to 10,experienced for at least one month

  • Maintenance therapy with hormone therapy or other maintenance therapy (trastuzumab, bevacizumab...) is allowed before and/or during the study (exceptfor pembrolizumab, abemaciclib and PARP inhibitors, which are not authorized)

  • Patient 18 years of age or older

  • Effective contraception in women of childbearing age

  • Patient affiliated to a social security plan

  • Signed informed consent

Exclusion

Exclusion Criteria:

  • Other identified causes of fatigue (anemia of grade > 2, underlying chronicdisease known to be associated with fatigue)

  • Ongoing chemotherapy (patients scheduled for oral capecitabine ortrastuzumab-emtasin in the adjuvant setting are not eligible)

  • Metastatic breast or gynecological cancer

  • Ongoing treatment with a tyrosine kinase inhibitor or other P-gp transportedmolecule or Pembrolizumab or PARP inhibitors

  • Patient requiring oral diabetes therapy

  • Regular intake of Vitamin C (in addition to what is provided by the diet)

  • Patients with chronic pain requiring daily treatment with analgesics,anti-inflammatory drugs or corticosteroids

  • Consumption of ginseng-based products in the month prior to inclusion

  • Hypersensitivity to any of the components of Qiseng or placebo

  • Pregnant or breastfeeding patient

  • Simultaneous participation in another therapeutic clinical trial (trial using anexperimental product)

  • Patient deprived of liberty, under guardianship or curatorship

  • Patient unable to undergo the medical follow-up of the trial for geographical,social or psychopathological reasons

  • History of any other malignant disease during the last 3 years, except for skincancer other than melanoma, carcinoma in situ of the uterus. Any other solid tumoror lymphoma (without bone marrow involvement) must have been treated and show nosigns of recurrence for at least 3 years

Study Design

Total Participants: 354
Treatment Group(s): 2
Primary Treatment: PLACEBO
Phase:
Study Start date:
September 27, 2022
Estimated Completion Date:
September 30, 2027

Connect with a study center

  • ARCOCEA_Clinique Europe

    Amiens,
    France

    Site Not Available

  • Ch Bayeux

    Bayeux,
    France

    Site Not Available

  • Centre Pierre Curie

    Beuvry,
    France

    Site Not Available

  • Centre François Baclesse

    Caen,
    France

    Active - Recruiting

  • Polyclinique du Parc

    Caen,
    France

    Site Not Available

  • Ch Calais

    Calais,
    France

    Active - Recruiting

  • Ch Cherbourg

    Cherbourg,
    France

    Site Not Available

  • Clinique de Flandre

    Coudekerque-Branche,
    France

    Active - Recruiting

  • Centre Henri Becquerel

    Rouen,
    France

    Active - Recruiting

  • Clinique des Dentellières

    Valenciennes,
    France

    Active - Recruiting

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