QISENG
Dietary Supplement2 capsules/day for 8 weeks.
NCT Number: NCT05241405
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
Interested in participating?
Request Info18 year and older
Female
Interventional
Not applicable
ARCOCEA_Clinique Europe, Amiens, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
2 capsules/day for 8 weeks.
2 capsules/day for 8 weeks.
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
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
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
Time frame: 4 and 8 weeks of treatment and 4 weeks after the end of treatment
EORTC QLQ-C30 quality of life questionnaire scores
Time frame: after 4 and 8 weeks of treatment, and 4 weeks after the end of treatment
HADS anxiety and depression questionnaire scores
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,
Time frame: after 4 and 8 weeks of treatment, and again 4 weeks after the end of treatment
measured by the IPAQ questionnaire scores
Time frame: after 4 and 8 weeks of treatment and 4 weeks after the end of treatment
measured by CAT-sleep questionnaire scores
Time frame: over a period of 8 weeks
measured by the total number of times the treatment was taken
Contact information is provided by the study sponsor or research team.
Alexandra LECONTE
CONTACT
Carine SEGURA, MD
CONTACT
Centre Francois Baclesse
Other
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
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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