Clinical trial Recruiting at 1 site Interventional Ages 40 to 80

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 typeInterventional
Ages40 Years to 80 Years
SexAll
Enrollment240 (estimated)
SponsorTel-Aviv Sourasky Medical Center
Government
Locations1 site (Tel Aviv)
StatusRecruiting
StartedJuly 1, 2026
Main results expectedDecember 31, 2028
Study endsDecember 31, 2028
Registry record updatedSeptember 24, 2026
Trial IDNCT07629869 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

  • Tel Aviv Sourasky Medical Center, Tel Aviv, 6423906
    Tel Aviv, Israel
    Recruiting

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.