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BIOLOGICAL EXPLORATION OF THE VASCULAR FRACTION FROM THE ADIPOSE TISSUE OF PATIENTS WITH SCLERODERMIA

BIOLOGICAL EXPLORATION OF THE VASCULAR FRACTION FROM THE ADIPOSE TISSUE OF PATIENTS WITH SCLERODERMIA IN THE CONTEXT OF THE DEVELOPMENT OF AN INNOVATIVE CELLULAR THERAPY FOR THE TREATMENT OF FUNCTIONAL HANDICAP OF THE HAND

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03629002
Acronym
sclerabio
Enrollment
30
Registered
2018-08-14
Start date
2018-09-30
Completion date
2020-09-30
Last updated
2018-08-14

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

Conditions

Systemic Scleroderma

Brief summary

The overall objective is to propose a comprehensive analysis of the biological properties of the stromal vascular fraction evaluated in the SCLERADEC 2 clinical trial (n = 15 available) and preserved in the biological collection, compared to healthy donors (n = 10). This characterization will focus on the exploration of the phenotypic and functional characteristics of the main cellular subpopulations present in the stromal vascular fraction of scleroderma patients likely to be associated with a better regenerative vascular or anti-fibrotic activity of the cell therapy product. The main objective will be to validate whether the supposed mechanism of action of this innovative therapy, in relation to the representativity of the endothelial progenitors, carrying the vascular regeneration activity, is preserved in the sclerodermic context. A total of 30 subjects (20 systemic Scleroderma patients and 10 healthy donors) will be included.

Interventions

BIOLOGICALStudy of the gene expression profile

qPCR analysis

Sponsors

Assistance Publique Hopitaux De Marseille
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

Patients with systemic scleroderma: * fulfilling the inclusion criteria for the SCLERADEC 2 trial: patients with systemic Scleroderma older than 18, desiring a therapeutic alternative and having a functional impotence authenticated by a functional index of Cochin's hand greater than 20. * having given their consent for the constitution of a sample in the biological collection * having completed the follow-up visit to M3 of the SCLERADEC 2 study to have responder / non-responder status. Healthy volunteers: * having recourse to a liposuction operation for aesthetic reasons, * with a BMI between 18 and 27, * not declaring chronic diseases, * having signed the non-opposition

Exclusion criteria

Patients with systemic scleroderma: * Body mass index (weight-to-height ratio squared) less than 18 * Major Sclerodactyly objectified by Rodnan score applied by hand\> 16 (out of a total of 18 points) * Severe tendon retraction of the fingers objectified by a defect extension in passive measure in goniometry\> 90 ° C for at least 2 proximal interphalangeal joints * Digital infection (including infected ulcer, ulcer with local inflammatory signs and clinical suspicion of osteitis) * Pulmonary arterial hypertension and / or progressive and / or oxygen-dependent pulmonary fibrosis * Prescription of a new systemic treatment for Systemic Scleroderma in the month prior to inclusion * Persons infected with HIV, HCV, HBV, HTLV and syphilis * Patients on immunosuppressants outside corticosteroid therapy \<10 mg / day and methotrexate * Known hypersensitivity to human albumin For healthy patients and volunteers: * Contraindication to surgery (patients on anticoagulant or antiaggregant, disorders of haemostasis, contraindication to the analgesic protocol used) * Premenopausal women of childbearing age without contraception * Minors * Pregnant or lactating women * Majors protected by law (under tutorship or curatorship) * Persons staying in a health or social facility * People in emergency * Persons deprived of their liberty * Inmates * Non-beneficiaries of a social security scheme * Absence or refusal of non-opposition

Design outcomes

Primary

MeasureTime frameDescription
Study of the gene expression profile18 monthsStudy of the gene expression profile by qPCR

Secondary

MeasureTime frameDescription
Phenotypic analysis of the cells composing the stromal vascular fraction18 monthsPhenotypic analysis performed by flow cytometry after multiple immunolabelings (CD90, CD14, CD146, CD34, CD45, DRAQ5, NucBlue Fixed Cell Stain (DAPI)) performed in accordance with the recommendations of the International Society for Cellular Therapy (ISCT) and IFATS.
Cell culture of the stromal vascular fraction to isolate and expand two populations of interest18 monthsMesenchymal stem cells (MSCs) obtained by culturing the total stromal vascular fraction without an immunomagnetic selection step.

Countries

France

Contacts

Primary ContactJérémy MAGALON
jeremy.magalon@ap-hm.fr
Backup ContactAlexandra GIULIANI
drci@ap-hm.fr04 91 38 27 47

Outcome results

None listed

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