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This document outlines the protocol for a Phase II multi-center, double-blind, randomized controlled clinical trial aimed at evaluating the efficacy and safety of a combination therapy involving pirfenidone and mofetil in patients with scleroderma-related interstitial lung disease. The study seeks to investigate improvements in lung function over an 18-month period, while monitoring tolerability and adverse effects.
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How to fill out scleroderma lung study iii

01
Review the study eligibility criteria to ensure compliance.
02
Gather necessary medical records related to scleroderma and lung conditions.
03
Contact the study coordinator for enrollment procedures.
04
Complete any required screening tests or questionnaires.
05
Schedule appointment times for follow-up assessments and treatments as asked.
06
Provide informed consent before participating in the study.

Who needs scleroderma lung study iii?

01
Patients diagnosed with scleroderma who are experiencing lung-related complications.
02
Individuals with a clinical diagnosis of interstitial lung disease associated with scleroderma.
03
Patients seeking new treatment options or participating in research to advance understanding of scleroderma lung disease.
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The Scleroderma Lung Study III is a clinical trial aimed at evaluating the effects of treatment on lung function and quality of life in patients with scleroderma-related lung complications.
Patients diagnosed with scleroderma who are participating in the clinical trial are required to file the necessary documentation for the Scleroderma Lung Study III.
Participants must complete the required forms by providing their medical history, current treatments, and any relevant health information as instructed by the study coordinators.
The purpose of the Scleroderma Lung Study III is to determine the effectiveness of new treatments for improving lung function and managing symptoms in patients with scleroderma.
Participants must report their medical history, current medications, pulmonary function test results, and any side effects experienced during the trial.
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