Interstitial Lung Disease Trial, Recruiting NCT07236541 Sponsor: Ming Zhong Condition: Interstitial Lung Disease
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Interstitial Lung Disease Trial, Recruiting

NCT07236541
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:

  • You must be 18 years of age or older
  • You are scheduled to have surgery to fully remove a lung cancer tumor, and after surgery the tissue is confirmed to be primary lung cancer (cancer that started in the lung)
  • During surgery, doctors are able to collect a sample of healthy lung tissue that is at least 5 cm away from the tumor
  • Case group: Before surgery, a breathing test confirmed you have COPD (a lung condition where airflow is limited, shown by a specific breathing test result)
  • Control group: Your breathing test results before surgery are normal and you have no history of COPD
  • You are able to understand and sign a consent form agreeing to take part in the study

Who may not be able to join:

  • You have been diagnosed with certain other lung conditions, such as scarring of the lung tissue (interstitial lung disease, pulmonary fibrosis, or lung scarring caused by dust exposure or tuberculosis)
  • You currently have an active lung infection, such as bacterial pneumonia, a fungal infection, or active tuberculosis
  • You have already received chemotherapy or radiotherapy before surgery, which could affect the lung tissue being studied
  • You have a serious immune system deficiency, or you have been taking high-dose steroid medication (or similar immune-suppressing drugs) for more than 4 weeks
  • You have another serious illness, such as severe heart failure or advanced kidney disease, that could affect your ability to take part or your life expectancy
  • You are pregnant or breastfeeding
  • You are unwilling to sign the consent form, or the researcher believes it would not be appropriate for you to join the study

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

Phone: 18359181031

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
Sponsor
Ming Zhong
Registry
ClinicalTrials.gov
Start date
30 October 2025
Est. completion
30 June 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Clarify the relationship between airway mucus embolism and secondary pulmonary fibrosis in COPD patients

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