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Recruiting NCT05098704

Preventive Effect of Clopidogrel on the Systemic Sclerosis Development Risk

Phase II / Phase III Interventional Scleroderma Systemic Sclerosis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: clopidogrel treatment, Placebo.
Who it may be relevant to
Registry conditions: Scleroderma, Systemic Sclerosis. Basic parameters: 18 years — 85 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Phase II/III Double-blind Randomized Placebo-controlled Trial Assessing the Preventive Effect of Clopidogrel on the Systemic Sclerosis Development Risk in Subjects With Specific Dysimmunity and Raynaud Phenomenon

Overview

Systemic sclerosis (SSc) is a severe autoimmune disease associating dysimmunity, vasculopathy and fibrosis. No curative treatment is available. Pre-clinical abnormalities can be found such as specific autoantibodies. The association of Raynaud phenomenon and SSc-specific anti-nuclear antibodies is the hallmark of pre-scleroderma subjects, among who around 47% declare a complete disease after five years. The aim of this study is to assess in this particular population the preventive effect of an anti-platelet treatment.

Detailed description

In this study, platelet activation is targeted as it could play a key role in the pathogenesis of SSc. It has been shown in several publications that platelets are activated in SSc with a correlation between the level of activation and disease activity. Secondary to this activation, soluble and membrane effectors were increased, and induced vascular damages and fibrosis. The results obtained in the laboratory (CNRS UMR-5164) directly involved platelets in this mechanism by inducing the thymic stromal lymphopoietin (TSLP) production by endothelial cells and by showing the pro-fibrotic effect of TSLP. In vivo data in SSc murine model recently obtained, confirmed the preventive role on fibrosis of clopidogrel. The early control of this platelet activation could prevent the course of events leading to SSc.

The therapeutic strategy assessed in this study will be the oral administration of clopidogrel (75 mg per day) during two years to subjects presenting an association of specific dysimmunity and Raynaud phenomenon (RP). The administration of clopidogrel will be double-blinded versus placebo.

Subjects will be included and treated during a 2-year period and will be followed for a period of 36 months after treatment, i.e. a total of 60 months. The follow-up will be every six months mainly comprising clinical examination, patient reported outcomes and blood sampling.

Interventions

  • Drug clopidogrel treatment
    75 mg daily during 24 months
  • Drug Placebo
    75 mg daily during 24 months

Primary outcome measures

  • Frequency of occurrence of SSc at 5 years according to American College of Rheumatology (ACR) / European League Against Rhumatism (EULAR) 2013 criteria in the two randomization groups [Time frame: 60 months after baseline (Day 0)]
Secondary outcome measures (11)
  • Frequency of occurrence of cutaneous fibrosis (sclerodactyly or other affected area) clinically assessed by at least 2 independent investigators in the two randomization groups [Time frame: 60 months after baseline (Day 0)]
  • Mean of modified Rodnan skin score (which varies between 0 and 51, with higher values mean higher disease severity) in the two randomization groups. [Time frame: 60 months after baseline (Day 0)]
  • Mean of Cochin hand function scale (which varies between 0 and 90, with higher values mean higher disease severity) in the two randomization groups. [Time frame: 60 months after baseline (Day 0)]
  • Proportion of sex ratio at inclusion in the two randomization groups. [Time frame: At baseline (Day 0)]
  • Mean age at inclusion in the two randomization groups. [Time frame: At baseline (Day 0)]
  • Proportion of patients exposed to toxic products at inclusion in the two randomization groups. [Time frame: At baseline (Day 0)]
  • Proportion of patients exposed to toxic products at 5 years in the two randomization groups. [Time frame: 60 months after baseline (Day 0)]
  • Proportion of patients affected by a limited form of SSc at 5 years in the two randomization groups. [Time frame: 60 months after baseline (Day 0)]
  • Proportion of patients affected by a diffuse form of SSc at 5 years in the two randomization groups. [Time frame: 60 months after baseline (Day 0)]
  • Proportion of patients presenting a specific antibody positivity (anti-scl70, anti-centromere) in the two randomization groups at inclusion. [Time frame: At baseline (Day 0)]
  • Proportion of patients presenting megacapillaries by capillaroscopy at 5 years in the two randomization groups. [Time frame: 60 months after baseline (Day 0)]

Eligibility criteria

Inclusion criteria

  • Patient over 18 years old, and less than 85 years old.
  • Patient with positive AAN (AAN ≥ 1/160) with the following specificity: anti-Scl70 or anti-centromere or anti-RNApolIII, or any other auto-antibodies related to systemic sclerosis
  • Patient with RP reported by the subject and confirmed by the physician.
  • Patient affiliated to a health insurance system.
  • Patient who accepts to participate to the study and signs an inform consent form.

Exclusion criteria

  • Patient with an SSc diagnosis according to ACR/EULAR 2013 criteria.
  • Patient with skin fibrosis at screening.
  • Patient with antiplatelet treatment at screening.
  • Patient with contraindications to clopidogrel.
  • Patient treated by immunosuppressive agent at screening.
  • Patient treated by anticoagulants at screening
  • Pregnant or breastfeeding women.
  • Women of childbearing age refusing effective contraception method during the study treatment (24 months).
  • Incompetent adults (i.e. Individuals under the protection of a conservator)

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Triple blind
Primary purpose
Treatment

Study locations

France · 11 centers
  • CH de la Cote Basque - service de rhumatologie — Bayonne
  • CHU de Bordeaux - service de Médecine Interne et Maladies Infectieuses — Bordeaux
  • CHU de Bordeaux - service de rhumatologie — Bordeaux
  • CHU de Brest - service de rhumatologie — Brest
  • CHU de Grenoble Alpes - service de médecine vasculaire — Grenoble
  • CH de Libourne - service de rhumatologie — Libourne
  • CH de Mont-de-Marsan - service de rhumatologie — Mont-de-Marsan
  • AP-HP - Hôpital Cochin - service de médecine interne — Paris
  • … and 3 more centers

Identifiers

NCT: NCT05098704 · CHUBX 2017/45 · 2024-511005-39-00

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗