COPD flare-up clinic after severe COPD attacks
Official title: The Role of COPD Flare-up Clinic Service After Severe Exacerbations to Reduce Recurrent Exacerbations
Run by Tel-Aviv Sourasky Medical Center · NCT07629869 · Data updated 2026-11-12
This trial tests whether follow-up in a dedicated flare-up clinic helps people after a COPD flare-up compared with usual follow-up calls.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 40 Years to 80 Years |
| Sex | All |
| Enrollment | 240 (estimated) |
| Sponsor | Tel-Aviv Sourasky Medical Center Government |
| Locations | 1 site (Tel Aviv) |
| Status | Recruiting |
| Started | July 1, 2026 |
| Main results expected | December 31, 2028 |
| Study ends | December 31, 2028 |
| Registry record updated | September 24, 2026 |
| Trial ID | NCT07629869 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults with a prior COPD diagnosis who recently had an acute exacerbation and can attend in-person clinic visits and telephone follow-ups.
✕Probably not a fit
Patients who cannot participate in in-person follow-ups or have exclusionary conditions may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
In this randomized study, adults with COPD who have had an acute exacerbation and either were discharged from the emergency department or hospitalized are assigned to a structured flare-up clinic follow-up or standard telephone follow-up for 12 months. The main goal is to see if the clinic reduces the rate of moderate to severe COPD flare-ups over a year. Secondary outcomes include long-term COPD and comorbidity management, quality of life, and mortality. Allocation is 1:1 and stratified by index-visit disposition, using centralized concealed randomization.
Why it matters
Potential benefit: If successful, participants may experience fewer COPD flare-ups and improved overall COPD care and quality of life.
How similar studies have gone: Previous similar approaches have shown that structured post-exacerbation care can improve outcomes in COPD, though the effect size varies by setting.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Prior COPD diagnosis based on clinical and spirometry accepted criteria. * Acute exacerbation of COPD as the main reason for ED arrival. * Ability to perform in-person and telephone follow-up. * Agree to participate, with a signed informed consent. Exclusion Criteria: * Symptomatic heart failure as the main reason for emergency department visit in the last 6 months. * Uncontrolled comorbidity. * Vulnerable Populations: To ensure ethical compliance and participant safety, the study will exclude vulnerable populations. This includes pregnant women, and any person lacking the mental or legal capacity to provide independent informed consent.
Where it's running
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Tel Aviv Sourasky Medical Center, Tel Aviv, 6423906
Tel Aviv, Israel Recruiting
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.