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NCT06844344Recruiting

Diagnosing peRipheral Lung Lesions With CRYO Biopsies

Source: ClinicalTrials.gov · Last updated 20 May 2026

Brief summary (registry, in English)

Lung cancer is the leading course of cancer related deaths world-wide. Lung cancer screening will increase the number of small lung lesion in need of biopsy to confirm the diagnosis. Obtaining lung biopsies with a bronchoscopy has the lowest risk of complications (1-2%) compared to other modalities such as transthoracic needle biopsy (20%), however diagnostic yield needs improvement. Currently a diagnosis is established in 50- 70% of the bronchoscopic procedures depending on the step-up. One way to improve the yield would be by using a cryo probe through the bronchoscope which freezes a small part of the lung for extraction, and thereby provides larger biopsies for examination. This will increase the chances of obtaining sufficient material from a small lesion to determine the diagnosis. The DR CRYO study will compare cryo biopsies to forceps biopsies for the diagnosis of peripheral lung lesions. We hope that the cryo biopsies can improve the diagnostic capabilities of bronchoscopy and provide better biopsies for tumor marker analyses. The project is relevant both for patients undergoing diagnostic work-up for lung cancer in early stages .

Status (registry)
Recruiting
Study type
Interventional
Enrollment
100 (estimated)
First submitted
23 Jan 2025
Start date
1 Mar 2025
Primary completion date
1 Feb 2027
Lead sponsor
Odense University Hospital
Diseases
Lung cancer
NCT number
NCT06844344

What you commit to

  • Study type: Interventional
  • Planned participants: 100
  • From 1 Mar 2025 to the primary completion date, 1 Feb 2027
  • 2 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

  • \- Pregnancy
  • Not able to provide informed consent.

Who the study is looking for

  • \- Patients undergoing diagnostic work-up for lung cancer due to a lung lesion surrounded by normal lung tissue (identified by CT)
  • Age 18 or above
  • Bronchoscopy with planned forceps sampling from the lesion

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

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Næstved Hospital
Coordinator of this site? Confirm its status
NæstvedDenmarkNot yet recruiting
Odense University Hospital
Coordinator of this site? Confirm its status
OdenseDenmarkRecruiting

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