Clinical trial · Interventional
Cannabics Capsules as Treatment to Improve Cancer Related CACS in Advanced Cancer Patients
Cannabics Capsules as Treatment to Improve Cancer Related Cachexia and Anorexia Syndrome in Advanced Cancer Patients- Pilot Study
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The main purpose in the treatment of patients with advanced cancer and cancer anorexia cachexia syndrome (CACS) is to prolong life and to improve quality of life (QoL) as far as possible. QoL in patients with CACS is directly related to loss of appetite and loss of weight. Cannabis pills are given in Israel to advanced cancer patients with various symptoms in order to improve their QoL. There is data on safety/toxicity of cannabis, and these pills are given under the regulations of the Israel Ministry of Health. The purpose of this study is to examine the influence of Cannabics capsules on improving loss of appetite and loss of weight.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Atypical Anorexia Nervosa | — | UNRESOLVED | — |
| Cancer Cachexia | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Cannabics capsules | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Cannabics 5mg
- description
- Patients will be treated initially for 3-4 days with 1x5mg Cannabics capsules per day for gradual adaptation. From the 5th day, patients will be treated 2x5mg capsules per 24 hours for a period of 3 months. However, since some patients may suffer from side effects mainly, dizziness and or anxiety, dosage for these patients will be reduced to 5mg per day.
- interventionNames
- Other: Cannabics capsules
Primary outcomes (1)
- measure
- weight gain of ≥10% from baseline weight assessed.
- timeFrame
- 3 months
- description
- weight gain of ≥10% from baseline weight assessed by weighing the patient every two weeks in the first month, every month in the coming two months, and every six weeks in the next three months
Secondary outcomes (7)
- measure
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Age above 18 years 2. Histological evidence of an incurable malignancy 3. Estimated life expectancy ≥3 months 4. Performance status ≤2 (ECOG classification) 5. Self-report of weight loss of at least 3kg during the preceding 2 months and/or a dietitian-estimated caloric intake of less than 20 calories/kg of body weight per day 6. Patient believes that loss of appetite or loss of weight is an ongoing problem for him 7. Use of chemotherapy or radiotherapy is permitted 8. Sign of written informed consent Exclusion Criteria: 1. Ongoing use of tube feedings or parental nutrition 2. Edema or ascites 3. Central nervous system metastases or brain tumors (patients with stable disease in the brain 28 days after treatment can be included in the study) 4. Treatment with adrenal corticosteroids (except for short-term dexamethasone during time of chemotherapy), androgens, progestational agents or other appetite stimulants within the previous two weeks 5. Insulin-requiring diabetes 6. Pregnancy or lactation or unwillingness to use oral contraceptives 7. Other life-threatening medical conditions 8. Anticipated alcohol or barbiturate use during the study period 9. Mechanical obstruction of the alimentary tract, malabsorption, or intractable vomiting 10. Use of cannabis or synthetic cannabinoids in the last four weeks
References
Publications (1)
- DERIVEDBar-Sela G, Zalman D, Semenysty V, Ballan E. The Effects of Dosage-Controlled Cannabis Capsules on Cancer-Related Cachexia and Anorexia Syndrome in Advanced Cancer Patients: Pilot Study. Integr Cancer Ther. 2019 Jan-Dec;18:1534735419881498. doi: 10.1177/1534735419881498. PMID 31595793