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Recruiting NCT07491523

Double Immunosuppression With or Without Anti-fibrotic in Scleroderma ILD

Observational SSc-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: Antifibrotic drugs (nidanib or pirfenidone), MMF Immunosuppression.
Who it may be relevant to
Registry conditions: SSc-Systemic Sclerosis. Basic parameters: from 18 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
Greece
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Patients with ssc-ild receiving double immunosuppression with or without anti fibrotic tratment

Detailed description

Systemic sclerosis (scleroderma) is a rare systemic autoimmune disease. It primarily affects the skin, but it can also involve other vital organs and systems, and is characterized by fibrosis, vascular abnormalities, and the production of autoantibodies. Its main pathological feature is the excessive production and deposition of collagen in the skin and other organs.

Mortality in scleroderma varies depending on the type and severity of the disease, particularly on whether vital organs are involved. Patients with limited cutaneous scleroderma generally have a better prognosis and life expectancy, whereas those with diffuse scleroderma face a higher risk of death from disease-related complications, mainly due to lung involvement.

Pulmonary involvement in scleroderma is common, either affecting the pulmonary blood vessels (pulmonary hypertension) or the supporting structure (interstitium) of the lungs, leading to interstitial fibrosis.

Objective:

The aim of the study is to compare patients receiving only dual immunosuppressive therapy (control group) with patients receiving dual immunosuppressive therapy combined with antifibrotic treatment (e.g., nintedanib).

Methods:

This will be a retrospective study including patients with scleroderma and diffuse pulmonary fibrosis who are followed at the Rheumatology Department of the University General Hospital of Patras and are receiving the two proposed treatment regimens. Because fibrosis and its progression are slow processes, we propose a comparative analysis of outcomes in both groups at 2 years from treatment initiation.

Inclusion criteria:

Presence of pulmonary fibrosis (documented by chest HRCT), regardless of whether pulmonary function tests show a restrictive pattern or not.

Availability of pulmonary function tests for each patient at the following time points:

0 months (baseline) 6 months 12 months Patients (controls) should be receiving either dual therapy (MMF + RTX) or triple therapy (MMF + RTX + nintedanib).

Analysis:

Statistical analysis will be performed using the unpaired two-tailed Student's t-test.

Expected results / originality / contribution to science:

To date, no similar study exists in the international literature. Since interstitial lung disease is the leading cause of death in patients with scleroderma, the results of this study may contribute to improved management. We hypothesize that the combination of dual immunosuppressive therapy and antifibrotic treatment will be superior to dual immunosuppressive therapy alone.

Interventions

  • Drug Antifibrotic drugs (nidanib or pirfenidone)
    Ssc - ild
  • Drug MMF Immunosuppression
    we will compare patients with SSc-ILD taking RTX and mmf and patients that are taking RTX,mmf and nintedanib

Primary outcome measures

  • pulmonary function test [Time frame: From enrollment till the end of study -1 years later]

Eligibility criteria

Inclusion Criteria:ild-ssc with double immunosuppression

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Exclusion criteria

  • ssc without ild

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

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Greece · 1 center
  • University of patras — Pátrai

Identifiers

NCT: NCT07491523 · University of Patra

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗