Preventive Effect of Clopidogrel on the Systemic Sclerosis Development Risk (PSSIT)
Primary Purpose
Scleroderma, Systemic Sclerosis
Status
Recruiting
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
clopidogrel treatment
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Scleroderma focused on measuring systemic sclerosis, clopidogrel, platelet, prevention, primary care
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)
Sites / Locations
- CHU de Bordeaux - service de rhumatologieRecruiting
- CHU de Brest - service de rhumatologie
- CH de Libourne - service de rhumatologie
- CHU de Limoges - Service de médecine interne
- CH de Mont-de-Marsan - service de rhumatologie
- CHU de Montpellier - service de médecine vasculaire
- AP-HP - Hôpital Cochin - service de médecine interne
- CH de Pau - service de médecine interne
- CHU de Toulouse - service de médecine interne
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
clopidogrel
placebo
Arm Description
Outcomes
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
Secondary Outcome Measures
Frequency of occurrence of cutaneous fibrosis (sclerodactyly or other affected area) clinically assessed by at least 2 independent investigators in the two randomization groups
Mean of modified Rodnan skin score (which varies between 0 and 51, with higher values mean higher disease severity) in the two randomization groups.
Mean of Cochin hand function scale (which varies between 0 and 90, with higher values mean higher disease severity) in the two randomization groups.
Proportion of sex ratio at inclusion in the two randomization groups.
Mean age at inclusion in the two randomization groups.
Proportion of patients exposed to toxic products at inclusion in the two randomization groups.
Proportion of patients exposed to toxic products at 5 years in the two randomization groups.
Proportion of patients affected by a limited form of SSc at 5 years in the two randomization groups.
Proportion of patients affected by a diffuse form of SSc at 5 years in the two randomization groups.
Proportion of patients presenting a specific antibody positivity (anti-scl70, anti-centromere) in the two randomization groups at inclusion.
Proportion of patients presenting megacapillaries by capillaroscopy at 5 years in the two randomization groups.
Full Information
NCT ID
NCT05098704
First Posted
October 4, 2021
Last Updated
October 17, 2022
Sponsor
University Hospital, Bordeaux
Collaborators
Ministry for Health and Solidarity, France
1. Study Identification
Unique Protocol Identification Number
NCT05098704
Brief Title
Preventive Effect of Clopidogrel on the Systemic Sclerosis Development Risk
Acronym
PSSIT
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
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
June 22, 2022 (Actual)
Primary Completion Date
June 2029 (Anticipated)
Study Completion Date
June 2029 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Bordeaux
Collaborators
Ministry for Health and Solidarity, France
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Scleroderma, Systemic Sclerosis
Keywords
systemic sclerosis, clopidogrel, platelet, prevention, primary care
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Model Description
placebo-controlled trial
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
90 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
clopidogrel
Arm Type
Experimental
Arm Title
placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
clopidogrel treatment
Intervention Description
75 mg daily during 24 months
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
75 mg daily during 24 months
Primary Outcome Measure Information:
Title
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 Measure Information:
Title
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)
Title
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)
Title
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)
Title
Proportion of sex ratio at inclusion in the two randomization groups.
Time Frame
At baseline (Day 0)
Title
Mean age at inclusion in the two randomization groups.
Time Frame
At baseline (Day 0)
Title
Proportion of patients exposed to toxic products at inclusion in the two randomization groups.
Time Frame
At baseline (Day 0)
Title
Proportion of patients exposed to toxic products at 5 years in the two randomization groups.
Time Frame
60 months after baseline (Day 0)
Title
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)
Title
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)
Title
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)
Title
Proportion of patients presenting megacapillaries by capillaroscopy at 5 years in the two randomization groups.
Time Frame
60 months after baseline (Day 0)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
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)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marie-Elise TRUCHETET, Prof
Phone
05.56.79.55.56
Ext
+33
Email
marie-elise.truchetet@chu-bordeaux.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Thomas BARNETCHE, PhD
Email
thomas.barnetche@chu-bordeaux.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marie-Elise TRUCHETET, Prof
Organizational Affiliation
CHU Bordeaux
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Linda WITTKOP, MD
Organizational Affiliation
University of Bordeaux
Official's Role
Study Chair
Facility Information:
Facility Name
CHU de Bordeaux - service de rhumatologie
City
Bordeaux
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marie-Elise TRUCHETET, Prof
Email
marie-elise.truchetet@chu-bordeaux.fr
First Name & Middle Initial & Last Name & Degree
Thomas BARNETCHE, PhD
Email
thomas.barnetche@chu-bordeaux.fr
First Name & Middle Initial & Last Name & Degree
Marie-Elise TRUCHETET, Prof
First Name & Middle Initial & Last Name & Degree
Joel CONSTANS, Prof
First Name & Middle Initial & Last Name & Degree
Pierre DUFFAU, Prof
First Name & Middle Initial & Last Name & Degree
Julien SENESCHAL, Prof
First Name & Middle Initial & Last Name & Degree
Estibaliz LAZARO, Prof
Facility Name
CHU de Brest - service de rhumatologie
City
Brest
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alain SARAUX, Prof
Email
alain.saraux@chu-brest.fr
First Name & Middle Initial & Last Name & Degree
Alain SARAUX, Prof
Facility Name
CH de Libourne - service de rhumatologie
City
Libourne
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jean-Philippe VERNHES, MD
Email
philippe.vernhes@ch-libourne.fr
First Name & Middle Initial & Last Name & Degree
Jean-Philippe VERNHES, MD
Facility Name
CHU de Limoges - Service de médecine interne
City
Limoges
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anne-Laure FAUCHAIS, Prof
Email
anne-laure.fauchais@unilim.fr
First Name & Middle Initial & Last Name & Degree
Anne-Laure FAUCHAIS, Prof
Facility Name
CH de Mont-de-Marsan - service de rhumatologie
City
Mont-de-Marsan
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marion MIRABEL, MD
Email
marion.mirabel@ch-mdm.fr
First Name & Middle Initial & Last Name & Degree
Marion MIRABEL, MD
Facility Name
CHU de Montpellier - service de médecine vasculaire
City
Montpellier
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pierrick HENNETON, MD
Email
p-henneton@chu-montpellier.fr
First Name & Middle Initial & Last Name & Degree
Pierrick HENNETON, MD
Facility Name
AP-HP - Hôpital Cochin - service de médecine interne
City
Paris
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Benjamin CHAIGNE, MD
Email
benjamin.chaigne@aphp.fr
First Name & Middle Initial & Last Name & Degree
Benjamin CHAIGNE, MD
Facility Name
CH de Pau - service de médecine interne
City
Pau
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xavier DELBREL, MD
Email
xavier.delbrel@ch-pau.fr
First Name & Middle Initial & Last Name & Degree
Xavier DELBREL, MD
Facility Name
CHU de Toulouse - service de médecine interne
City
Toulouse
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Grégory PUGNET, MD
Email
pugnet.g@chu-toulouse.fr
First Name & Middle Initial & Last Name & Degree
Grégory PUGNET, MD
12. IPD Sharing Statement
Learn more about this trial
Preventive Effect of Clopidogrel on the Systemic Sclerosis Development Risk
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