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NCT05411809Not yet recruiting

The ctDNA for Evaluating Whether to Use Adjuvant Therapy After SBRT in Patients With Early Lung Cancer

Source: ClinicalTrials.gov · Last updated 9 Jun 2022 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The purpose of this study is to determine whether ctDNA could help to evaluate whether to use drug adjuvant therapy after SBRT in patients with early lung cancer.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
180 (estimated)
First submitted
25 May 2022
Start date
Jun 2022
Primary completion date
Jun 2024
Lead sponsor
Peking University Third Hospital
Diseases
Lung cancer
NCT number
NCT05411809

What you commit to

  • Study type: Interventional
  • Planned participants: 180
  • From Jun 2022 to the primary completion date, Jun 2024
  • 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

  • Patients with factors that affect oral medication (such as cannot swallow, chronic diarrhea and intestinal obstruction, etc.) or intravenous medication;

Other illness

  • Patients with small cell lung cancer (including small cell carcinoma and non-small cell carcinoma mixed lung cancer);
  • Patients with any other severe and/or uncontrolled disease;
  • Patients with a history of psychotropic medicine abuse and cannot quit or have mental disorders;
  • Patients with disease which will severely endanger their security and could not complete this study, according to the judgement of researchers;

Who the study is looking for

  • Patients pathologically diagnosed as non-small cell lung cancer, and was early stage(AJCC 8th);
  • Patients aged between 18 -80 years; with expected survival time\>3 months.
  • Patients with normal organ function within 30 days prior to treatment, the following criteria are met:
    • blood routine examination criteria : i) hemoglobin (HB) ≥90g/L; ii) absolute neutrophil count (ANC) ≥1.5×10e9/L; iii) platelet (PLT) ≥80×10e9/L; b) biochemical tests meet the following criteria: i) total bilirubin (TBIL) ≤1.5 times of upper limit of normal (ULN); ii) alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤2.5 ULN; iii) serum creatinine (Cr) ≤1.5 ULN or creatinine clearance (CCr) ≥60mL/min;

Age in the registry: 18 years to 80 years · 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
Department of Radiation Oncology Cancer Center, Peking University Third Hospital 49# North Garden Rd.,Haidian Dist.
Coordinator of this site? Confirm its status
BeijingChinaUnknown status

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