Skip to content

Oral Medicinal Cannabis (CBD:THC) as Add-On to Standard of Care for Symptomatic and Palliative Treatment in Cancer Patients - a Multicentre Prospective Patient Registry in Switzerland and Germany.

Oral Medicinal Cannabis (CBD:THC) as Add-On to Standard of Care for Symptomatic and Palliative Treatment in Cancer Patients - a Multicentre Prospective Patient Registry in Switzerland and Germany. - Swiss CanOn - Swiss Cannabis Oncology

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00028190
Enrollment
100
Registered
2022-03-04
Start date
2022-03-20
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

cancer related symptoms and/or chemotherapy or radiation therapy related symptoms (e.g. chemotherapy-induced nausea and vomiting, pain, sleep problems, appetite loss)

Interventions

Group 1: Patients with cancer related and/or chemotherapy or radiation therapy related symptoms are regularly asked about symptoms, concomitant medication use, and quality of life.

Sponsors

Stiftung Swiss Tumor Institute
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Written informed consent; - Adult male and female patients > 18 years suffering from cancer related and/or chemotherapy or radiation therapy related symptoms; - Patients who have not been previously treated with a medical cannabis product for cancer related and/or chemotherapy or radiation therapy related symptoms but now are scheduled for a treatment with cannabinoids; - Using the consilium careTM App on their personal smartphone (Android or iOS system) as part of the routine medical data assessment; - No cognitive impairment as judged by the treating physician; - Ability to read and answer questions in German.

Exclusion criteria

Exclusion criteria: Patients who are in the opinion of the investigator unsuitable for participation in the registry for any other reason not listed in the inclusion and exclusion criteria.

Design outcomes

Primary

MeasureTime frame
To get insights from therapy with CBD:THC products added to SoC for supportive and palliative treatment of cancer related and/or chemotherapy or radiation therapy related symptoms in daily clinical practice under real world conditions.

Secondary

MeasureTime frame
Developing a data pool for future research questions. Capturing patient data continuously during medical cannabis-treatment to get insights on: - treatment pathways, - duration of medical cannabis treatment, - proportion of chemotherapy patients for whom guideline-compliant treatment of CINV is insufficient, - proportion of patients suffering from further cancer related and/or chemotherapy or radiation therapy related symptoms, - proportion of cancer patients receiving cannabis in total and per center, - proportion of patients for whom cannabis results in relief of their symptoms, - reasons for withdrawal from medical cannabis therapy, - information on related symptoms, e.g., appetite loss, anxiety, pain and sleep problems, - change in concomitant medications, - development of quality of life, - data on optimal dose titration.

Countries

Switzerland

Contacts

Public ContactAndreas Trojan

Onkologie See-Spital Horgen

andreas.trojan@see-spital.ch+41447281537

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026