- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07281534
Test-Retest Reliability of Cardiopulmonary Exercise Testing With Echocardiography (REPEATCPETecho)
December 12, 2025 updated by: Ziekenhuis Oost-Limburg
Analysing the Test-Retest Reliability of Cardiopulmonary Exercise Testing With Echocardiography
CPETecho is progressively employed in diagnostic settings for pathophysiological detection, offering comprehensive assessment of both pulmonary and cardiac functions.
This technique evolves from its invasive counterpart, where a diagnostic catheter is employed for hemodynamic monitoring, by substituting the invasive component with non-invasive echocardiography.
Nevertheless, data on the test-retest reliability of CPETecho remain sparse, a factor critical in differentiating between measurement effects and actual therapeutic impacts.
Study Overview
Study Type
Interventional
Enrollment (Estimated)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Philippe Bertrand, MD, PhD
- Phone Number: 0032471626094
- Email: philippe.bertrand@zol.be
Study Contact Backup
- Name: Sebastiaan Dhont, MD
- Phone Number: 0032471626094
- Email: sebastiaan.dhont@zol.be
Study Locations
-
-
-
Genk, Belgium, 3600
- Recruiting
- Ziekenhuis Oost-Limburg
-
Contact:
- Dhont Bertrand, MD, PhD
- Phone Number: 0471626094
- Email: sebastiaan.dhont@zol.be
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Capable of performing a maximal exercise test.
- Provide signed and dated informed consent.
Exclusion Criteria:
- Unstable symptoms, whereby therapy cannot be delayed for a week.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Single arm
Repeat CPET echo with a one-week interval
|
repeat CPETecho with a one-week interval
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Correlation coefficient (ICC)
Time Frame: Up to 2 weeks
|
Analysing the Test-Retest Reliability of Cardiopulmonary Exercise Testing with Echocardiography
|
Up to 2 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 1, 2025
Primary Completion (Estimated)
March 1, 2026
Study Completion (Estimated)
June 1, 2026
Study Registration Dates
First Submitted
February 26, 2024
First Submitted That Met QC Criteria
December 12, 2025
First Posted (Actual)
December 15, 2025
Study Record Updates
Last Update Posted (Actual)
December 15, 2025
Last Update Submitted That Met QC Criteria
December 12, 2025
Last Verified
November 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Z-2024011
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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