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The Effect of Cannabis in Pancreatic Cancer

The Effect of Medical Cannabis Inpatients With Palliative Pancreatic Cancer

Status
Withdrawn
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03245658
Enrollment
0
Registered
2017-08-10
Start date
2017-10-06
Completion date
2018-10-06
Last updated
2023-12-18

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

Conditions

Appetite Loss, Cachexia; Cancer, Cannabis, Morbidity, Mortality, Neoplasms Pancreatic, Palliative Medicine

Brief summary

Cannabinoids are known to increase appetite, but THC components have psychogenic properties too. CBD is the main component in the plant, and have only minimal psychogenic effects. The aim was to test the appetite stimulating effects of CBD in patients with pancreatic cancer in palliative treatment.

Detailed description

Randomization of consecutive patients who wanted to participate to a daily dose of CBD or not as a supplement to the standard treatment.

Interventions

DRUGTHC and CBD Mixture

Individually titrated doses on daily basis

Sponsors

Jens Rikardt Andersen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Adult, palliative pancreatic cancer diagnosis, weight loss \> 5%, understand and read Danish.

Exclusion criteria

* Regular use of cannabis, psychiatric disorders, alcohol abuse, life expectancy \< 6 months

Design outcomes

Primary

MeasureTime frameDescription
Energy and protein intakeThe outcome measure will be assessed at day 0 and at week 4Dietary history (% of estimated needs - NRS 2002)

Secondary

MeasureTime frameDescription
Appetite 1The outcome measure will be assessed at day 0 and at week 4VAS (cm on 10 cm scale)
Appetite 2The outcome measure will be assessed at day 0 and at week 4Dietary history (VAS (cm on 10 cm scale))
Appetite 3The outcome measure will be assessed at day 0 and at week 4EORTC QLQ-C30 (score, standard for the Quality of Life entity)
Appetite 4The outcome measure will be assessed at day 0 and at week 4EORTC QLQ-PAN26 (score, standard for the Quality of Life entity)
Quality of life 1The outcome measure will be assessed at day 0 and at week 4EORTC QLQ-C30 (score, standard for the Quality of Life entity)
Lean body massThe outcome measure will be assessed at day 0 and at week 4Bioimpedance (% of body weight, kg)
Quality of life 3The outcome measure will be assessed at day 0 and at week 4VAS (VAS (cm on 10 cm scale))
Pain 1The outcome measure will be assessed at day 0 and at week 4EORTC QLQ-C30 (score, standard for the Quality of Life entity)
Pain 2The outcome measure will be assessed at day 0 and at week 4EORTC QLQ-PAN26 (score, standard for the Quality of Life entity)
Pain 3The outcome measure will be assessed at day 0 and at week 4VAS (VAS (cm on 10 cm scale))
Mortality (8 weeks)8 weeksPatient records, national register
Quality of life 2The outcome measure will be assessed at day 0 and at week 4EORTC QLQ-PAN26 (score, standard for the Quality of Life entity)

Countries

Denmark

Outcome results

None listed

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