COPD Trial, Recruiting NCT05033990 Sponsor: University of Massachusetts, Worcester Condition: COPD
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COPD Trial, Recruiting

NCT05033990
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:

  • Healthy control group (40 people): People aged 30–55 with no history of smoking, vaping, or cannabis use (fewer than 100 cigarettes in their lifetime), and whose breathing test results are within the normal range, and who score below 10 on a standard airway symptom questionnaire.
  • "GOLD 0" group (roughly one-third of 960 participants): People aged 30–55 who have smoked at least 10 pack-years, and whose breathing test results are within normal range after using a bronchodilator (a medication that opens the airways).
  • "PRISm" group (roughly one-third of 960 participants): People aged 30–55 who have smoked at least 10 pack-years, whose airway-to-lung ratio on a breathing test is normal after a bronchodilator, but whose overall airflow is below 80% of what is expected for someone their age and size.
  • "GOLD 1–2" group (roughly one-third of 960 participants): People aged 30–55 who have smoked at least 10 pack-years, and whose breathing tests after a bronchodilator show a reduced airway-to-lung ratio but still at least 50% of expected airflow — consistent with early-to-moderate COPD.

Who may not be able to join:

  • People with severe asthma, defined as currently being on high-level asthma medication (confirm with trial site for specific medication thresholds), or having had three or more unplanned medical visits for asthma in the past 12 months, or having been hospitalised for asthma in the past 12 months.
  • People currently taking part in another clinical trial where the treatment being given is kept secret (blinded).
  • People who are pregnant at the time of the first study visit, or who plan to become pregnant during the study — this is due to the risk of radiation exposure from CT scans to an unborn baby.
  • People with cognitive difficulties that would prevent them from completing the study tasks.
  • People with a BMI (body mass index) above 35 at the start of the study, as higher body weight can affect the quality of CT scan images.
  • People with a lung condition other than COPD or asthma — such as interstitial lung disease or pulmonary fibrosis — or another condition that a doctor believes is the main cause of their breathing symptoms.
  • People with an illness that is expected to be life-limiting within the next three years.
  • People with any metal implants or devices in the upper body that could interfere with CT scan image quality.
  • People who have had radiation treatment to the chest, or chest surgery that involved removing lung tissue.
  • People with a known HIV/AIDS diagnosis.
  • People currently misusing illicit substances (marijuana is excluded from this criterion).
  • People with a history of, or who currently use, intravenous (IV) Ritalin.
  • People with a history of, or who currently use, heroin.
  • People who have used illegal intravenous drugs within the last 10 years, or who have used illegal intravenous drugs on more than 5 occasions at any point in their life.

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 14 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: Fernando J Martinez, MD, MS, University of Massachusetts, Worcester

Phone: 9199623266

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
University of Massachusetts, Worcester
Registry
ClinicalTrials.gov
Start date
8 September 2021
Est. completion
1 May 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

PRM fSAD

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: 14 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