NCT07506889Not yet recruiting
Simplified Exercise-based Risk Assessment in Lung Cancer
EXercise-based Evaluation of Ventilatory Efficiency for enHanced Risk Assessment in Lungcancer trEatment Using End-tidal CO2: a Multicenter, Prospective Study
Source: ClinicalTrials.gov · Last updated 8 Apr 2026
Brief summary (registry, in English)
Physiological evaluation is part of the preoperative risk estimation in patients with lung cancer, and it aids in the choice of treatment. Ventilatory efficiency during exercise has emerged as a strong predictor of major postoperative complications, so far determined during a maximal cardiopulmonary exercise test. However, this test is limited by its availability and high cost, due to the requirement of high-technological equipment and advanced expertise. The current project aims to evaluate a simplified and accessible method for risk evaluation before decision on treatment in lung cancer. It builds on recent advances in technology and knowledge and combines a simple, low-intensity cycling test with measurement of ventilatory efficiency (end-tidal carbon dioxide pressure) with a handheld monitor. In a prospective, multi-center design the investigators will include patients evaluated for suspected lung cancer. The main objective is to establish threshold values for end-tidal carbon dioxide associated with low respectively high risk of major complications in patients undergoing surgery. In addition, the study aims to determine if end-tidal carbon dioxide can predict severe side-effects during neoadjuvant or curatively aiming systemic therapy. The project is closely linked to clinical practice, and the results can be easily implemented due to the simple and cost-efficient methodology. the suggested simplified approach would also allow access to physiological evaluation where more advanced methods are unavailable.
- Status (registry)
- Not yet recruiting
- Study type
- Observational
- Enrollment
- 500 (estimated)
- First submitted
- 26 Mar 2026
- Start date
- 1 Apr 2026
- Primary completion date
- Dec 2029
- Lead sponsor
- Linkoeping University
- Diseases
- Lung cancer
- NCT number
- NCT07506889
What you commit to
- Study type: Observational
- Planned participants: 500
- From 1 Apr 2026 to the primary completion date, Dec 2029
- 5 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- Not able to perform cycle ergometer exercise
- Not able to understand spoken or written Swedish
Who the study is looking for
- Lung Cancer Diagnosis
- Age of at least 18 years
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (5)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Department of Pulmonology, Ryhov Coordinator of this site? Confirm its status | Jönköping | Sweden | Unknown status |
| Department of Pulmonology, Kalmar County Hospital Coordinator of this site? Confirm its status | Kalmar | Sweden | Unknown status |
| Department of Pulmonology, Blekinge Hospital Coordinator of this site? Confirm its status | Karlskrona | Sweden | Unknown status |
| Department of Pulmonology, University Hospital Coordinator of this site? Confirm its status | Linköping | Sweden | Unknown status |
| Department of Clinical Physiology Coordinator of this site? Confirm its status | Lund | Sweden | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.