Interstitial Lung Disease Trial, Recruiting NCT07541638 Sponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCS Condition: Interstitial Lung Disease
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Interstitial Lung Disease Trial, Recruiting

NCT07541638
Recruiting Not Applicable

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 26 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

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

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
7 November 2024
Est. completion
30 June 2026

Where this trial is recruiting

🇮🇹 Italy

Primary endpoints

Serum EV characteristics according to ILD presence

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov