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NCT Number: NCT05241405

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

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

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

ARCOCEA_Clinique Europe, Amiens, France

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with localized breast or gynecological cancer treated as curative adjuvant and/or neoadjuvant chemotherapy and/or adjuvant radiotherapy. These treatments must have 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 (except for 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 criteria

  • Other identified causes of fatigue (anemia of grade > 2, underlying chronic disease known to be associated with fatigue)
  • Ongoing chemotherapy (patients scheduled for oral capecitabine or trastuzumab-emtasin in the adjuvant setting are not eligible)
  • Metastatic breast or gynecological cancer
  • Ongoing treatment with a tyrosine kinase inhibitor or other P-gp transported molecule 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 an experimental 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 skin cancer other than melanoma, carcinoma in situ of the uterus. Any other solid tumor or lymphoma (without bone marrow involvement) must have been treated and show no signs of recurrence for at least 3 years

Treatment and study plan

QISENG

Dietary Supplement

2 capsules/day for 8 weeks.

Placebo

Dietary Supplement

2 capsules/day for 8 weeks.

Primary outcomes

  1. Fatigue score change [min :5; max:20]

    Time frame: After 1 week and 4 weeks after the end of treatment (so 8 weeks of treatment)

    The difference between the initial (inclusion) score and the best score based on EORTC QLQ-FA12 questionnaire (physical fatigue dimension) between assessments at 1 week (S9) and 4 weeks (S12) after the end of treatment) will be calculated

Secondary outcomes

  1. Other dimensions of fatigue [min :12; max:48]

    Time frame: after 4 weeks of treatment, after 8 weeks of treatment and 4 weeks after the end of treatment

    Score of emotional fatigue, cognitive fatigue, global score, according to the EORTC QLQ-FA12 self-questionnaire

  2. The incidence of treatment-related adverse events

    Time frame: up to 8 weeks after the end of treatment

    The incidence of treatment-related adverse events and the number of patients in whom at least one treatment-related adverse event occurred

  3. Quality of life level assessed by EORTC QLQ-C30 questionnaire

    Time frame: 4 and 8 weeks of treatment and 4 weeks after the end of treatment

    EORTC QLQ-C30 quality of life questionnaire scores

  4. anxiety level

    Time frame: after 4 and 8 weeks of treatment, and 4 weeks after the end of treatment

    HADS anxiety and depression questionnaire scores

  5. Cognitive function

    Time frame: after 4 and 8 weeks of treatment and 4 weeks after the end of treatment

    Cognitive function dimensions, according to the FACT-Cog self-assessment questionnaire,

  6. Physical activity level

    Time frame: after 4 and 8 weeks of treatment, and again 4 weeks after the end of treatment

    measured by the IPAQ questionnaire scores

  7. Sleep quality

    Time frame: after 4 and 8 weeks of treatment and 4 weeks after the end of treatment

    measured by CAT-sleep questionnaire scores

  8. The level of acceptability of the treatment,

    Time frame: over a period of 8 weeks

    measured by the total number of times the treatment was taken

Study contacts

Contact information is provided by the study sponsor or research team.

Alexandra LECONTE

CONTACT

[email protected]

Carine SEGURA, MD

CONTACT

[email protected]

+33231455050

Sponsors and collaborators

Lead sponsor

Centre Francois Baclesse

Other

Collaborators

  • Groupement Interrégional de Recherche Clinique et d'Innovation
  • NATSUCA laboratory

Registry information

Official study title

Evaluation of the Impact of Taking American Ginseng for 8 Weeks on Fatigue in Patients Treated for Localized Breast or Gynecological Cancer - Randomized, Placebo-controlled, Double-blind Study

Acronym: QISEIN

Important dates

Study start
2022
Primary completion
2027
Study completion
2027
First posted
Feb 15, 2022
Registry last updated
Oct 1, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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