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Skin involvement for Systemic Sclerosis (PCTS Trial)

N/A
Waitlist Available
Research Sponsored by University of West London
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year
Awards & highlights

PCTS Trial Summary

Systemic Sclerosis (SSc) is an autoimmune connective tissue disease characterized by autoantibodies, fibrosis and microvascular injury and endothelial cell activation that results in vascular damage. Vascular injury induces both innate and acquired immune responses resulting in fibroblast activation and organ fibrosis. SSc may target multiple organs, including: skin, lungs, heart, vascularization, kidneys, the gastrointestinal tract and musculoskeletal structures. Mortality among scleroderma patients is significant, with a 3.5 standardized mortality ratio (SMR) in studies of prevalent cases. This mortality may be increased in the early years of the disease, reaching a SMR of 4 in a multinational inception cohort. In general, treatment strategies target involved organs as early as possible to avoid damage. Many treatment options are available for each manifestation, but evidence with respect to the order of treatment is scarce. Financial costs, the lack of proper outcome measures, difficulty to recruit patients as a rare disease, all prevent the development of new big clinical trials, oppositely to other common diseases such as stroke or cancer. The heterogeneous features of SSc may make trials challenging. The current guidelines available are the British guidelines (2017) , and the updated European League Against Rheumatism (EULAR) guidelines, published in 2017. Management guidelines have some gaps regarding second-line treatment, combinations and there are no proposed algorithms. With the pragmatic trials, the investigators intend to fill the gap between the complicated randomized clinical trials and the observational studies. Using the treatments that have already been proved useful in SSc, in an open-label randomized way and based on some refined expert-made algorithms, will allow the investigators to establish the order in how to use them. Patients will be offered to participate with the collection of their clinical data and, if they give their consent, they will be randomized according to the algorithms. There will be an optional part of the study consisting in the collection of blood samples and skin samples for future research.

Eligible Conditions
  • Systemic Sclerosis
  • Systemic Scleroderma

PCTS Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year
This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 year for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Bleeding
Constipation visual analog scale
Diarrhea visual analog scale
+8 more

PCTS Trial Design

10Treatment groups
Experimental Treatment
Group I: Skin involvementExperimental Treatment1 Intervention
Group II: Raynaud's phenomenonExperimental Treatment1 Intervention
Group III: Pulmonary arterial hypertensionExperimental Treatment1 Intervention
Group IV: PainExperimental Treatment1 Intervention
Group V: Interstitial lung disease inductionExperimental Treatment1 Intervention
Group VI: Inflammatory arthritisExperimental Treatment1 Intervention
Group VII: Gastroesophageal refluxExperimental Treatment1 Intervention
Group VIII: Digital ulcersExperimental Treatment1 Intervention
Group IX: ConstipationExperimental Treatment1 Intervention
Group X: Bacterial overgrowthExperimental Treatment1 Intervention

Find a Location

Who is running the clinical trial?

University of Western Ontario, CanadaOTHER
164 Previous Clinical Trials
318,846 Total Patients Enrolled
University of West LondonLead Sponsor
2 Previous Clinical Trials
90 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~62 spots leftby Apr 2025