Fact CheckerSign in

NCT04976296Recruiting

MRD Monitoring in Lung Cancer After Resection

Dynamic Molecular Residual Disease Detection in Stage I-IIIA Non-Small Cell Lung Cancer After Radical Resection

Source: ClinicalTrials.gov · Last updated 17 Mar 2022 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The conception of molecular residual disease (MRD) extending from hematologic tumor to solid tumors. Evidences supporting MRD evaluation for lung cancer by liquid biopsy has gradually accumulated, especially circulating tumor DNA (ctDNA). In this observational study, the investigators prospectively enroll stage I-IIIA non-small cell lung cancer (NSCLC) patients who underwent complete resection. Preoperative blood sample, tumor tissue and dynamic postoperative blood samples are collected continuously for MRD detection. This study aim to explore the prognostic value of MRD for stage I-IIIA NSCLC patients after complete resection.

Status (registry)
Recruiting
Study type
Observational
Enrollment
300 (estimated)
First submitted
19 Jul 2021
Start date
1 Sept 2021
Primary completion date
30 Dec 2027
Lead sponsor
Guangdong Provincial People's Hospital
Diseases
Lung cancer
NCT number
NCT04976296

What you commit to

  • Study type: Observational
  • Planned participants: 300
  • From 1 Sept 2021 to the primary completion date, 30 Dec 2027
  • 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.

Prior treatment

  • Rx, R1 or R2 resection

Other illness

  • History of other malignant tumors within 5 years

Other

  • Mixed small cell and NSCLC histology

Who the study is looking for

  • Diagnosis of histologically confirmed NSCLC (WHO 2015 classification) with resectable (stage I-IIIA) disease.
  • Complete resection
  • Age ≥18 years at the time of screening
  • Capable of giving signed 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
Guangdong Lung Cancer Institute & 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.