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An Observation Placebo-controlled Trial with Cannabidiol Added-on Standard Treatment for Thai Patients Suffering from Psoriasis

An Observation Placebo-controlled Trial with Cannabidiol Added-on Standard Treatment for Thai Patients Suffering from Psoriasis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20220208003
Enrollment
70
Registered
2022-02-08
Start date
2022-03-01
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

Psoriasis patients with mild to moderate severity Psoriasis, Cannabidiols, CBD

Interventions

Psoriasis patients with CBD as an adjuvant (Active group),Psoriasis patients without CBD as an adjuvant (Control group)
Treatment,Treatment
Psoriasis patients with CBD (Active),Psoriasis patients without CBD (Control)

Sponsors

Faculty of Medicine, Western University
Lead Sponsor
National Research Council of Thailand
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. A patient who has been diagnosed with psoriasis, treated in the outpatient department of Nawamin Hospital, aged 18 years and over, both male and female. 2. Psoriasis patient group with mild disease severity (PASI score less than 3) or psoriasis patients with moderate disease severity (PASI score 3-10) 70 patients 3. BSA value less than 90 4. No complications from other diseases such as severe skin infections. No psoriatic arthritis conditions, cardiovascular disease. 5. Patients with normal LFT, AST (SGOT) and ALT (SGPT) not more than 2 times normal. 6. RFT eGFR value more than 59 7. Able to speak, read, listen and understand Thai language 8. Willing to cooperate/voluntarily join the trial along with signing a written consent to participate in the research project

Exclusion criteria

Exclusion criteria: 1. Psoriasis patient group with a high degree of disease severity (PASI score more than 10) 2. BSA value more than 90 or increased by more than 2 times during treatment 3. LFT AST (SGOT), ALT (SGPT) greater than 2 times normal during treatment 4. RFT eGFR less than 59 (Stage 3a) during treatment. 5. Having complications from other diseases such as severe skin infections No psoriatic arthritis conditions, cardiovascular disease. 6. Patients who need to use group drugs Beta-Blockers and Oral Steroids or a history of medicinal cannabis use

Design outcomes

Primary

MeasureTime frame
Responder rate 3-6 months PASI score

Secondary

MeasureTime frame
Quality of life 3-6 months PGI-B, PGI-C, PBI-S, MOS SF12

Countries

Thailand

Contacts

Public ContactPornthep Siriwanarangsan

Faculty of Medicine, Western University

wandee.ta@western.ac.th0891916781

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026