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NCT06453889Not yet recruiting

Efficacy and Safety of Multimode Thermal Therapy in the Treatment of Early Peripheral Lung Cancer

Source: ClinicalTrials.gov · Last updated 12 Jun 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The purpose of the study is to evaluate the efficacy and safety of multimode thermal therapy for early peripheral lung cancer, and to explore the changes of systemic immune microenvironment after multimode thermal therapy.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
10 (estimated)
First submitted
25 May 2024
Start date
Jun 2024
Primary completion date
Jun 2025
Lead sponsor
Shanghai Chest Hospital
Diseases
Lung cancer
NCT number
NCT06453889

What you commit to

  • Study type: Interventional
  • Planned participants: 10
  • From Jun 2024 to the primary completion date, Jun 2025
  • 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 poor cardiopulmonary function or other comorbidities who cannot tolerate multimode thermal therapy;
  • Patients whose chest CT indicated that the lung lesions could not be reached through the chest wall through multimode thermal therapy;
  • Patients who have received other anti-tumor drugs or have used immune checkpoint inhibitors in the past 6 months;
  • Those who have undergone surgical operations or had allogeneic organ transplants within 1 month;
  • Long-term use of steroid;

Other illness

  • Poor control of malignant pleural effusion;
  • The patient has an uncontrolled disease (including but not limited to active infection, symptomatic congestive heart failure, unstable angina, arrhythmia, mental illness, etc.);
  • Primary immune deficiency or autoimmune diseases (e.g. rheumatoid arthritis, systemic lupus erythematosus, etc.);

Lab values

  • Severe liver and kidney function and coagulation function abnormalities, platelet count \<70×109/L;

Other

  • Pregnant and lactating women;
  • Other circumstances considered inappropriate for participation in this study.

Who the study is looking for

  • Age ≥18 years old;
  • Pathologically diagnosed as primary peripheral non-small cell lung cancer, preoperative staging suggested clinical staging as T1N0M0, stage IA (including new-onset lung cancer after surgery and multiple primary lung cancer);
  • The ECOG PS score is 0-2;
  • Expected survival ≥6 months;
  • Negative driver gene mutation: driver genes were defined as EGFR, ALK, ROS1, RET;
  • Agree to undergo multimode thermal therapy as initial treatment after being assessed unsuitable for surgery or refusing surgery, and sign 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
Shanghai Chest Hospital
Coordinator of this site? Confirm its status
ShanghaiChinaUnknown status

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