Interstitial Lung Disease Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Adults between 18 and 75 years old, both male and female, are eligible to be considered.
- People who have given their written agreement (informed consent) to take part.
- People who have a confirmed diagnosis of one of the following conditions: Systemic Sclerosis (SSc), Rheumatoid Arthritis (RA), Sjögren's Syndrome (SS), Inflammatory Muscle Disease (IIM), or Undifferentiated Connective Tissue Disease (UCTD), diagnosed according to internationally recognised medical standards.
- People whose blood test results show specific markers that indicate a higher risk of developing lung scarring (ILD), with the specific markers required depending on which condition has been diagnosed (confirm with trial site for details).
- People who have evidence of lung changes on a specialised lung scan (HRCT) showing that at least 10% of the lung tissue is affected, with the scan performed within the previous 6 weeks — or, for some participants, a recent scan showing no such changes may also be considered.
- People who are either not currently taking immune-suppressing medications, or who have been on a stable dose of such medications for at least three months before the relevant blood test is done.
Who may not be able to join:
- People currently taking corticosteroid medication (such as prednisone) at a dose higher than 10 mg per day.
- People who have received the medication rituximab within the past 24 weeks.
- People whose veins are difficult to access in a way that would make blood collection problematic.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Silvia Laura Bosello, Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Phone: +390630159650
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Serum EV characteristics according to ILD presence
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.