← Back to Clinical Trials
Recruiting NCT05008081

NCT05008081 The CATALINA Study

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT05008081
Status Recruiting
Phase
Sponsor Wim Janssens
Condition Chronic Obstructive Pulmonary Disease Exacerbation
Study Type OBSERVATIONAL
Enrollment 1,000 participants
Start Date 2022-10-25
Primary Completion 2027-03

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 1,000 participants in total. It began in 2022-10-25 with a primary completion date of 2027-03.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The CATALINA study is a prospective cohort study embedded within CICERO (Collaboration In COPD ExaceRbatiOns, a European Respiratory Society supported Clinical Research Collaboration), designed to collect standardised, longitudinal clinical data and biological samples in 20 centres across Europe and beyond.

Eligibility Criteria

Inclusion Criteria: * Age 18 years and older * Established diagnosis of COPD by medical doctor (based on clinical history OR pulmonary function test with an FEV1/FVC \< 0.7) * Current hospitalization with suspicion of an acute exacerbation of COPD (AECOPD) * Inclusion within 48 hours post hospital admission * Voluntary written informed consent of the participant or his/her representative obtained prior to any study procedure Exclusion Criteria: * Patients unwilling or unable to comply with study procedures * Patients not requiring treatment with systemic corticosteroids, antibiotics or both as a minimum therapy for the index AECOPD * Patients with a confirmed positive test result for COVID19, or those highly suspected based on clinical examination

Contact & Investigator

Central Contact

Kristina Vermeersch, PhD

✉ kristina.vermeersch@kuleuven.be

📞 016342284

Principal Investigator

Wim Janssens, MD, PhD

STUDY CHAIR

UZ/KU Leuven - Belgium

Frequently Asked Questions

Who can join the NCT05008081 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Chronic Obstructive Pulmonary Disease Exacerbation. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05008081 currently recruiting?

Yes, NCT05008081 is actively recruiting participants. Contact the research team at kristina.vermeersch@kuleuven.be for enrollment information.

Where is the NCT05008081 trial being conducted?

This trial is being conducted at Linz, Austria, Vienna, Austria, Brussels, Belgium, Leuven, Belgium and 11 additional locations.

Who is sponsoring the NCT05008081 clinical trial?

NCT05008081 is sponsored by Wim Janssens. The principal investigator is Wim Janssens, MD, PhD at UZ/KU Leuven - Belgium. The trial plans to enroll 1,000 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology