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NCT06494254Recruiting

Post-Operative Prediction of PulmonarY Function

Post-Operative Prediction of PulmonarY Function A Pilot Study to Assess the Benefit of Incorporating Regional Ventilation Information in the Prediction of Post-operative Lung Function for Lung Cancer Surgery

Source: ClinicalTrials.gov · Last updated 20 May 2026

Brief summary (registry, in English)

Prediction of postoperative lung function is currently based on anatomical segment counting (ASC), which incorporates pulmonary function test (PFT) results. Standard PFTs such as spirometry can only measure pulmonary capacity as an average over the entire lung and do not take regional function differences into account. Nuclear medicine is recommended where regional functional imaging is required to inform surgical decisions. However, nuclear medicine scans are expensive, time consuming and not available in all institutions. CT-ventilation imaging is a cheaper and more accessible alternative to nuclear medicine for informing lung cancer patient treatment choices. The primary aim is to quantify the difference between predicted postoperative values of pulmonary function metrics derived from CT ventilation imaging and standard anatomical segment counting method.

Status (registry)
Recruiting
Study type
Observational
Enrollment
15 (estimated)
First submitted
2 Jul 2024
Start date
25 Jun 2025
Primary completion date
Dec 2026
Lead sponsor
University of Sydney
Diseases
Lung cancer
NCT number
NCT06494254

What you commit to

  • Study type: Observational
  • Planned participants: 15
  • From 25 Jun 2025 to the primary completion date, 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

  • Interstitial lung disease.

Other

  • Pregnant women.

Who the study is looking for

  • Aged 18 years or older.
  • ECOG performance status 0-2.
  • Lung cancer surgical candidates.
  • Undergo SPECT V/Q scans within 8 weeks of registration.
  • Undergo BHCT scans within 8 weeks of registration.
  • Pulmonary function tests within 8 weeks of registration.
  • Willingness to give written informed consent.
  • Willingness and ability to comply with the study procedures and visit requirements.

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
Royal North Shore Hospital
Coordinator of this site? Confirm its status
Saint LeonardsAustraliaRecruiting

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