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Evaluation of the Efficacy and Safety of Cannabis Oil (Lung Dum, Koh Thao Formulation II) in Patients with Mild to Moderate Pain

Evaluation of the Efficacy and Safety of Cannabis Oil (Lung Dum, Koh Thao Formulation II) in Patients with Mild to Moderate Pain

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20250704002
Enrollment
50
Registered
2025-07-04
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

1. Mild to moderate non-specific pain (pain score between 1 to 7) 2. Does it has any Adverse Effects after using Cannabis oil (Lung Dam Koh Tao formulation II) Pain,Cannabis oil,Adverse EffectsI,Cannabis oil (Lung Dam Koh Tao formulation II)

Interventions

Patients experiencing mild to moderate pain associated with various medical conditions, such as cancer, palliative care patients, and individuals diagnosed with migraine.
Treatment
study group

Sponsors

Surat Thani Provincial Public Health Office
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients experiencing mild to moderate pain associated with various medical conditions, such as cancer, palliative care patients, and individuals diagnosed with migraine,2. Patients who have been diagnosed by a licensed modern medicine practitioner or a licensed Thai traditional medicine practitioner as requiring treatment with Lung Dam Koh Tao Cannabis Oil Formula 2,3. Patients without any of the following contraindications,Those with severe or unstable cardiopulmonary conditions, or who are at risk of cardiovascular disease,Patients with psychiatric disorders, Pregnant or breastfeeding women, Individuals with a known allergy to cannabis,Individuals with a history of substance abuse, including nicotine dependence or heavy alcohol consumption,Patients currently receiving anticoagulant therapy.

Exclusion criteria

Exclusion criteria: 1.Patients who experience severe adverse effects from the use of cannabis. 2.Patients who do not wish to continue participation in the study. 3.Patients who are unable to attend scheduled appointments or fail to return for follow-up evaluations with the Thai traditional medicine practitioner or applied Thai traditional medicine practitioner who prescribed the cannabis oil.

Design outcomes

Primary

MeasureTime frame
Pain Day 0 (baseline), Day 7, and at 1, 3, and 6 months following the initial visit (Day 0) Likert scale,Adverse Effects Day 0 (baseline), Day 7, and at 1, 3, and 6 months following the initial visit (Day 0) Adverse Event Assessment Form

Secondary

MeasureTime frame
Quality Of Life Day 0 (baseline), Day 7, and at 1, 3, and 6 months following the initial visit (Day 0) Edmonton Symptom Assessment System ,The 5-level EQ-5D version

Countries

Thailand

Contacts

Public Contactnoppol vanichjaroen

Surat Thani Provincial Public Health Office

ponthai2@gmail.com0993958175

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026