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Clinical Trial Summary

The goal is to explore whether the application of cannabis extract Avextra 10/10 solution is suitable to contribute to an improvement in the symptom burden and well-being of oncological palliative care patients. The primary objective of the study is to demonstrate the improvement in global symptom burden in the intervention arm compared to the placebo control group over a period of 12±2 days, as measured by a percentage change in the value of the Edmonton Symptom Assessment System total symptom distress score (ESAS TSDS) at baseline and after 12±2 days.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06097533
Study type Interventional
Source University Hospital Schleswig-Holstein
Contact
Status Not yet recruiting
Phase Phase 2/Phase 3
Start date December 1, 2023
Completion date November 30, 2026

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