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The Use of Cannabidiol in Cancer Patients

Prevalence of Cannabidiol (CBD) Consumption and Cancer Patients' Expectations in One Oncology Day-Hospital: A Cross-sectional Study and Questionnaire Validation

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05407298
Acronym
CANPADIOL
Enrollment
350
Registered
2022-06-07
Start date
2021-11-15
Completion date
2022-04-30
Last updated
2022-06-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer

Keywords

Cannabidiol, cancer patient

Brief summary

Alternative and complementary medicines (MAC) are commonly used by cancer patients to help them to face with anticancer treatment, reduce oncology symptoms and/or anticancer treatment adverse effects, detoxifying the body. In consistence with guidelines from the French Society for Oncology Pharmacy (SFPO), the pharmaceutical consultation includes a discussion and collection of herbs, botanical and other natural products consumed by cancer patients. This aim to prevent and manage herb-drug interaction as well as other drug-related problems (DRP). The recent French experimentation dedicated to cannabidiol for medical use could enhance interest of cancer patients in the field of MAC. However, cannabidiol have shown inhibitory effect on different cytochromes with a risk of HDI as other MAC. While the prevalence of MAC consumption is already known in some type of cancer, the consumption of CBD is less known and should be explored. Through this study we wish to know the prevalence of cannabidiol consumption in cancer patients and to establish a typical profile as well as to know the modalities of use. We also want to validate a questionnaire through a literacy scale.

Detailed description

* A Prospective observational study * Conducted in an oncology day-hospital (CHU de Reims) All data collected were: * Clinical characteristics, * Administrative data, * Medication review, * Biologic data collection, * Oncological data, * Disease data Statistical analysis: * Quantitative variables: described as mean ± standard deviation (SD) or median (Interquartile range and minimum and maximum) * Student test and Fischer exact performed to compare CBD users and non-users. * Analysis of variance: used to compare scores between different variables * Univariate logistic and multivariate logistic regressions were performed. Variables with a p-value \< 0.20 (Wald test) in the univariable analyses were considered eligible for the multivariable models.

Interventions

Non Applicable

Sponsors

CHU de Reims
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

All the patients (\>18yo) who received anticancer treatment

Exclusion criteria

* Patients who received anticancer drug with very short administration time (typically subcutaneous anticancer drugs as 5-azacitidine, bortezomib and some monoclonal antibodies) * Patients who were not able to speak and understand French as well as who were unable to communicate clearly.

Design outcomes

Primary

MeasureTime frame
Prevalence of CBD consummation among patients receiving anticancer treatmentDay 0

Secondary

MeasureTime frame
Knowledge assessment of cancer patients with the CBD medical use in the literacy scopeDay 0

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026