ClinicalTrials.Veeva

Menu

Intraoperative Frozen Section Pathology to Diagnose the IASLC Grades for Lung Adenocarcinoma (ECTOP-1014)

Fudan University logo

Fudan University

Status

Completed

Conditions

Surgical Procedure, Unspecified
Pathology
Lung Adenocarcinoma

Treatments

Procedure: Surgical resection

Study type

Observational

Funder types

Other

Identifiers

NCT05794698
CONCORD-A

Details and patient eligibility

About

This study is one of Eastern Cooperative Thoracic Oncology Projects (ECTOP-1014). The goal of this clinical trial is to confirm the concordance rate between intra-operative frozen section pathological diagnosis and post-operative paraffin embedded pathological diagnosis, and use this result to guide surgical treatment for early stage (cT1N0M0) lung adenocarcinomas.

Enrollment

827 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients who sign the informed consent form and are willing to complete the study according to the study protocol;
  • No previous history of cancer or pulmonary surgery;
  • Solitary lesions or multiple lesions with only one not manifesting as pure ground-glass opacity (GGO) on CT scan;
  • Peripheral clinical T1N0M0 patients that are eligible for surgery;
  • Non-small cell lung cancer is pathologically diagnosed before or at surgery;
  • No radiation therapy or chemotherapy before surgery.

Exclusion criteria

  • Patients with clinical stages other than T1N0M0;
  • The lesion cannot be completely resected;
  • Previous history of cancer;
  • Patients having received radiation therapy or chemotherapy.

Trial design

827 participants in 1 patient group

Study group
Description:
Clinical T1N0M0 lung adenocarcinoma patients eligible for surgery.
Treatment:
Procedure: Surgical resection

Trial contacts and locations

1

Loading...

Central trial contact

Yue Zhao, M.D., Ph.D.

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems