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A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Clinical Trial Evaluating the Safety and Efficacy of Bifidobacterium adolescentis for the Treatment of Psoriasis

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Clinical Trial Evaluating the Safety and Efficacy of Bifidobacterium adolescentis for the Treatment of Psoriasis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116047
Enrollment
Unknown
Registered
2026-01-05
Start date
2026-01-05
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Psoriasis

Interventions

Experimental Group: Apply 5 mL of Bifidobacterium adolescentis solution to psoriatic lesions on the limbs daily for a duration of 2 months.
Control Group: Apply 5 mL of heat-inactivated Bifidobacterium adolescentis solution to psoriatic lesions on the limbs daily for a duration of 2 months.
Placebo Control Group: Apply 5 mL of normal saline to psoriatic lesions on the limbs daily for a duration of 2 months.

Sponsors

Shenzhen People’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: PASI score (Psoriasis Area and Severity Index) < 10 (indicating mild to moderate disease) with psoriatic lesions present on the limbs; Provision of written informed consent and voluntary participation; Age between 18 and 60 years, in generally good health; No use of any psoriasis-related medications within the past 6 months; Absence of local infection or neuromuscular diseases.

Exclusion criteria

Exclusion criteria: Patients with no psoriatic lesions on the limbs, other types of psoriasis (e.g., pustular, erythrodermic, or arthropathic), or severe psoriasis (typically defined as PASI score = 10 or BSA = 10%); Patients with active concurrent skin diseases or severe comorbidities; Any other condition that, in the investigator's judgment, would render the participant unsuitable for the study (e.g., deemed unreliable, or unable/unwilling to comprehend or adhere to study procedures and assessments).

Design outcomes

Primary

MeasureTime frame
Trans Epidermal Water Loss;

Secondary

MeasureTime frame
Clinical photography;Dermoscopic imaging;

Countries

china

Contacts

Public ContactJianglin Zhang

Shenzhen People’s Hospital (The First Affiliated Hospital of Southern University of Science and Technology; The Second Clinical Medical College of Jinan University)

zhang.jianglin@szhospital.com+86 138 7314 3466

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026