Study on Safety and Efficacy of UCB-MNCs for Radiation-induced Lung Injury

Trial statusNot yet recruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexAll
Age18-75
SponsorZhejiang Cancer Hospital

About this trial

This study aims to evaluate the safety and efficacy of the umbilical cord blood mononuclear cells (UCB-MNCs) therapy for radiation-induced lung injuryr (RILI) by observing factors related to the therapeutic effect and adverse reactions of UCB-MNCs in treating RILI .

Eligibility criteria

Qualifiers

Ages 18-75 years,with no restriction on gender;

History of chest radiotherapy;

Diagnosed with grade 2-3 radiation-induced lung injury according to CTCAE 4.0 classification criteria in "Diagnosis and Treatment of Radiation-induced Lung Injury";

Inadequate response to conventional treatment for two weeks, with no relief or progressive worsening of symptoms;

Disqualifiers

Severe cardiac insufficiency (such as NYHA class III or IV), uncontrolled hypertension (systolic blood pressure ≥160mmHg or diastolic blood pressure ≥110mmHg);

Positive for hepatitis B, hepatitis C, human immunodeficiency virus (HIV), or syphilis;

ECOG score ≥2;

Currently participating in or participated in other clinical trials within 4 weeks;

Trial design

Treatments tested in this trial

  • UCB-MNCs

Treatment groups

10 Participants
are divided into 1 treatment group

Locations

This trial has no locations

Sponsors and collaborators