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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

Full criteria on ClinicalTrials.gov

Sites (5)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Department of Pulmonology, Ryhov
Coordinator of this site? Confirm its status
JönköpingSwedenUnknown status
Department of Pulmonology, Kalmar County Hospital
Coordinator of this site? Confirm its status
KalmarSwedenUnknown status
Department of Pulmonology, Blekinge Hospital
Coordinator of this site? Confirm its status
KarlskronaSwedenUnknown status
Department of Pulmonology, University Hospital
Coordinator of this site? Confirm its status
LinköpingSwedenUnknown status
Department of Clinical Physiology
Coordinator of this site? Confirm its status
LundSwedenUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.