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SCLERoderma et Adipose-DErived Stroma Cells

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02866552
Acronym
SCLERADECIII
Enrollment
44
Registered
2016-08-15
Start date
2017-01-31
Completion date
2019-08-31
Last updated
2016-08-15

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

Conditions

Systemic Sclerosis

Brief summary

Systemic sclerosis (SSc) is an auto-immune orphan disease mainly characterized by an alteration of the microvascular network, and by cutaneous and visceral fibrosis. Hands are frequently affected, as a consequence of ischemic phenomena and cutaneous fibrosis. As a result, patients suffer from everyday disability, with consequences on their occupational activities and social contact, sometimes severely altering their quality of life. To date, no anti-fibrosis treatment has proven effective; existing vasodilation treatments are unfortunately not very effective, and are associated with adverse effects or restrictions. It is consequently of utmost importance that an effective treatment for sclerodermic hands be developed. The injection of adipose autologous tissue is a common practice in plastic surgery, and has been known for over a century. Adipose tissue, originally used to increase volume, is also characterized by trophic properties associated to stromal vascular fraction (SVF), which contain multipotent stem cells, capable of tissue repair. Interestingly, some SVF cells can be angiogenic and anti-inflammatory, which could improve damage seen with SSc. The injection of SVF into the fingers would also make it possible to control the production of the extracellular matrix and to improve the balance between fibrosis and fibrolysis, resulting in an improvement of cutaneous sclerosis The main purpose is to evaluate the efficacy of SVF injections in the fingers of patients suffering from SSc on the Cochin hand functional scale evaluated at 12 months, in comparison to the control group.

Interventions

DRUGRinger lactate

Sponsors

Assistance Publique Hopitaux De Marseille
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Systemic Sclerosis ( limited or diffuse cutaneous shape) * Men and women of more than 18 years old * Patients wishing for a therapeutic alternative * Functional Disability of the dominant hand authenticated by a functional index of the hand of Cochin functional scale upper to 20

Exclusion criteria

* Body mass index (weight in kilograms divided by height in meters squared) lower than 18 * Finger infection (including infected ulcer, ulcer with signs of local inflammation and clinical suspicion of osteitis) * Contraindication to surgery * Prescription of a new systemic treatment for SSc in the month before the inclusion Subjects infected with HIV, HCV ( hepatitis C virus) , HBV (hepatitis B virus), HTLV ( human T-cell leukemia virus) and syphilis * Pre-menopausal women of reproductive age, taking no contraceptive method * Patients receiving immunosuppressive therapy not including corticosteroid therapy \< 10 mg/D and methotrexate

Design outcomes

Primary

MeasureTime frame
Cochin hand functional scale12 months

Secondary

MeasureTime frame
the severity (frequency and intensity of crises) of Raynaud's phenomenon12 months
the strength (Jamar et Pinch test)12 months
the trouble trophicity (health assesment questionnaire)12months
the pain in the hands (EVA pain scale),12 months

Countries

France

Contacts

Primary ContactBrigitte GRANEL
brigitte.granel@ap-hm.fr
Backup Contactalexandra GIULIANI
alexandra.giuliani@ap-hm.fr

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026