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NCT06215326Recruiting

Short-term Effects of Preoperative Exercise in Moderate-to-high Perioperative Risk Lung Cancer Patients

Short-term Effects of Preoperative Exercise in Moderate-to-high Perioperative Risk Lung Cancer Patients(PRE-EXELUCA): a Prospective Randomized Controlled Clinical Trial

Source: ClinicalTrials.gov · Last updated 3 Aug 2026

Brief summary (registry, in English)

The goal of this clinical trail is to compare the effects of preoperative exercise training of different intensities on short-term cardiorespiratory function and postoperative outcomes in patients scheduled for lung resections.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
100 (estimated)
First submitted
20 Dec 2023
Start date
23 Jan 2024
Primary completion date
31 Dec 2026
Lead sponsor
Guangdong Provincial People's Hospital
Diseases
Lung cancer
NCT number
NCT06215326

What you commit to

  • Study type: Interventional
  • Planned participants: 100
  • From 23 Jan 2024 to the primary completion date, 31 Dec 2026
  • 1 site 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 illness

  • Concurrent or previous history of other malignant tumors.
  • Dementia; infirmity; or inability to participate in sports (musculoskeletal limitations, namely, injuries, frailty, and weakness).
  • Irregular vital signs (heart rate: \< 40 or \> 120 bpm at rest; blood pressure: systolic blood pressure \> 200 mm Hg or diastolic pressure \> 110 mm Hg; T: ≥ 38.5 or ≤ 36◦C; SpO2 ≤ 90%).

Other

  • Life expectancy less than 1 year.
  • Inability to maintain exercise training.
  • Currently enrolling in any other clinical trials.
  • Patient refusal.

Who the study is looking for

  • Age\>18 years.
  • Suspected or confirmed primary lung cancer with scheduled surgical treatment.
  • Moderate-to-high perioperative risk, defined as FEV1\<60% of predicted value (wedge) or ppo FEV1\<60% of predicted value (lobectomy/segmentectomy) or VO2peak\<20 ml/kg/ min.
  • Sign informed consent and accept to comply with the requirements of the study protocol.
  • Completion of a baseline Complete cardiopulmonary exercise testing (CPET).

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Guangdong Provincial People's Hospital
Coordinator of this site? Confirm its status
GuangzhouChinaRecruiting

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