Skip to content

Safety and efficacy of cell therapy in psorisis

Safety and efficacy of injection of adipose tissue derived mesanchymal exosomes for skin lesions in patients with chronic plaque psoriasis

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT20080901001159N29
Enrollment
12
Registered
2020-10-05
Start date
2020-08-05
Completion date
Unknown
Last updated
2020-10-06

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

Conditions

Psoriasis. Psoriasis

Interventions

Intervention 1: Intervention First group: Single intra-dermal injection of 50 µg of exosomes derived from adipose tissue mesenchymal cells per cm2 of plaque into 0.5 ml of normal saline and follow up

Sponsors

Skin and Stem cell Research Center of Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Chronic plaque psoriasis for at least 6 months plaque Mild to severity of moderate (grade 1-3) PASI 3-12 No response to standard treatments No incidence of new lesion or increase in size of previous lesions during past 3 months

Exclusion criteria

Exclusion criteria: Other types of psoriasis include pustular, erythrodermic, gotate, and drug induced Immunosuppressive drugs over the past 4 weeks or topical medications other than moisturizing lotions in the 2 past weeks Severe underlying disease (including liver, kidney and heart failure), increased liver enzymes more than 3 times normal and creatinine more than 2 high and uncontrolled blood pressure Pregnancy or lactation diabetes mellitus Hepatitis B, C or HIV Patients with immunodeficiency Patients with malignancy Disabling disease Systemic or injection site infection

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: intervention start date up to 3 months. Method of measurement: Pain intensity scale.;Redness severity. Timepoint: intervention start date up to 3 months. Method of measurement: Physical examination.

Secondary

MeasureTime frame
Lesion severity (grade 1-3). Timepoint: Before intervention, every week up to 1 month, and every month up to 3 months. Method of measurement: evaluator assessment.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohamad Ali Mohseni Meybodi

Skin and Stem Cell Research Center, Tehran University of Medical sciences

alimohseni6154@gmail.com+98 21 2220 5158

Outcome results

None listed

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