Clinical trial Recruiting at 1 site Phase 2 Interventional Ages 16 to 60

Lactobacillus plantarum for adults with mild psoriasis

Official title: Evaluating the Safety and Efficacy of Lactobacillus Plantarum in Treating Psoriasis: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial

Run by Shenzhen People's Hospital · NCT07194200 · Data updated 2026-11-12

This study will test whether taking Lactobacillus plantarum or an inactivated version can improve skin symptoms in adults aged 18–60 with mild psoriasis.

Quick facts

PhasePhase 2
Study typeInterventional
Ages16 Years to 60 Years
SexAll
Enrollment184 (estimated)
SponsorShenzhen People's Hospital
Academic / other
Locations1 site (Shenzhen, Guangdong)
StatusRecruiting
StartedDecember 15, 2025
Main results expectedJune 25, 2026
Study endsJune 30, 2026
Registry record updatedDecember 24, 2025
Trial IDNCT07194200 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18–60 in good general health with mild plaque psoriasis (PASI <10), no recent medication use, and no other inflammatory skin or serious systemic diseases are the intended participants.

Probably not a fit

Patients with moderate-to-severe psoriasis, other psoriasis subtypes, active skin infections, major comorbidities, or who cannot comply with study procedures are unlikely to benefit from participation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This Phase 2, randomized, double-blind, placebo-controlled trial at Shenzhen People's Hospital will assign adults with mild psoriasis (PASI <10) to receive live Lactobacillus plantarum, inactivated Lactobacillus plantarum, or placebo. Participants must be 18–60 years old, in good general health, and off other medications for at least six months. The trial will monitor safety and changes in psoriasis severity and skin-related outcomes over the treatment period. The study is designed to explore whether modifying the skin microbiome can reduce inflammation and improve the skin barrier in psoriasis.

Why it matters

Potential benefit: If successful, this approach could provide a microbiome-targeted treatment that reduces psoriasis symptoms with potentially fewer systemic side effects than conventional systemic therapies.

How similar studies have gone: Early preclinical work and small clinical reports suggest microbiome modulation may help psoriasis, but randomized controlled evidence is still limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Reference to Psoriasis Area and Severity Index (PASI) score \< 10 Patients have been informed of the study details, voluntarily participate, and have signed the informed consent form; Aged 18-60 years with good general health status; No use of any medications within 6 months; No various inflammatory or immune skin diseases, no local infections, and no neuromuscular diseases.

Exclusion Criteria:

* Patients with other types of psoriasis or severe psoriasis; Those in the active phase of skin diseases or with other serious diseases; Other situations deemed unsuitable for enrollment by the researchers, such as subjects who are untrustworthy, unable to accept or understand the study assessments.

Where it's running

  • Shenzhen People's Hospital
    Shenzhen, Guangdong, China
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.