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NCT07488507Recruiting

Diagnostic Value and Safety of Combined Biopsy for Mediastinal Metastasis of Lung Cancer

Diagnostic Value and Safety of EBUS-TBNA Combined With Medaistinal Cryobiopsy for Mediastinal Metastasis of Lung Cancer

Source: ClinicalTrials.gov · Last updated 23 Mar 2026

Brief summary (registry, in English)

The study is aimed o evaluate the diagnostic performance and treatment guidance of endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) combined with transbronchial mediastinal cryobiopsy (EBUS-TBMCB) in patients with mediastinal metastases of lung cancer.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
240 (estimated)
First submitted
14 Mar 2026
Start date
20 Mar 2026
Primary completion date
1 Mar 2030
Lead sponsor
Third Military Medical University
Diseases
Lung cancer
NCT number
NCT07488507

What you commit to

  • Study type: Interventional
  • Planned participants: 240
  • From 20 Mar 2026 to the primary completion date, 1 Mar 2030
  • 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

  • Presence of severe cardiopulmonary disease, coagulation disorders, massive hemoptysis, poor tolerance to anesthesia, or other contraindications related to bronchoscopy;
  • Presence of mental illness, severe neurosis, or other conditions that preclude the provision of informed consent;
  • Any other conditions considered to be inappropriate to be involved in this trial.

Other

  • Intraoperative endobronchial ultrasound exploration of the lesion failed to detect the target lesion despite \> 20 minutes of attempts;
  • Lesions identified as abscesses or cysts;
  • Patients who have participated in other clinical trials within 3 months;

Who the study is looking for

  • Aged ≥18 years;
  • Presence of at least one mediastinal lesion (short-axis diameter ≥10 mm) confirmed by thin-slice chest CT;
  • Patients who have not undergone prior mediastinal biopsy and require further mediastinal biopsy to confirm etiology or pathological subtype, meeting at least one of the following criterias:
    • (1) suspected lung cancer diagnosed by two senior physicians; (2) confirmed lung cancer (requiring mediastinal staging); (3) recurrent lung cancer; 4.Patients must have completed all required preoperative laboratory tests and necessary examinations (e.g., cardiac ultrasound, CTA) to rule out contraindications; 5. Patients are informed and capable of providing written informed consent.

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
Third Military Medical University
Coordinator of this site? Confirm its status
ChongqingChinaRecruiting

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