Actively Recruiting

Phase 1
Phase 2
Age: 18Years - 80Years
All Genders
NCT05455034

Single-cell Sequencing of BLF to Guide the Treatment of Radiation Pneumonitis or Immune Checkpoint Inhibitor Pneumonitis

Led by Xinqiao Hospital of Chongqing · Updated on 2025-07-14

40

Participants Needed

1

Research Sites

126 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

A multicenter, exploratory clinical research, to map the radiation or immune checkpoint inhibitor pneumonitis in patients with alveolar lavage single-celled map. Find out the pathogenesis and prevention strategies of radiation or immune checkpoint inhibitor pneumonitis. Specific treatment is given based on the recommendation of the treatment guidelines for radiation or immune checkpoint inhibitor pneumonitis and the results of single cell sequencing, which will become a new technology for clinical application.

CONDITIONS

Official Title

Single-cell Sequencing of BLF to Guide the Treatment of Radiation Pneumonitis or Immune Checkpoint Inhibitor Pneumonitis

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Signed informed consent and able to follow the study protocol
  • Diagnosed with radiation pneumonitis or immune checkpoint inhibitor pneumonitis after radiotherapy or immunotherapy for non-small cell lung cancer, without prior glucocorticoid or other drug treatment
  • Age between 18 and 75 years
  • Eastern Cooperative Oncology Group performance status (ECOG PS) score of 0 to 3
  • No contraindications to bronchoalveolar lavage
Not Eligible

You will not qualify if you...

  • Poor compliance or violation of study rules
  • Liver or kidney dysfunction such as myocardial infarction, angina, or significantly elevated liver enzymes
  • Use of corticosteroids or immunosuppressive drugs within 14 days before enrollment
  • Severe infection or hospitalization due to infection within 4 weeks before enrollment
  • Active or severe chronic infections requiring systemic antibiotics within 14 days before enrollment
  • Untreated chronic hepatitis B, high HBV DNA levels, or active hepatitis C infection
  • Known HIV infection
  • Participation in another clinical trial or use of investigational drugs within 28 days before enrollment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Xinqiao Hospital

Chongqing, Chongqing Municipality, China, 400037

Actively Recruiting

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Research Team

J

Jianguo Sun, doctor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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