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Clinical study for the safety and efficacy of intratumoral injection of drug-packaging microparticles in the treatment of advanced lung adenocarcinoma under CT guidance

Clinical study for the safety and efficacy of intratumoral injection of drug-packaging microparticles in the treatment of advanced lung adenocarcinoma under CT guidance

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800020110
Enrollment
Unknown
Registered
2018-12-14
Start date
2018-12-10
Completion date
Unknown
Last updated
2019-01-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung cancer

Interventions

Case series:Intratumoral injection of drug-packaging microparticles

Sponsors

Xuanwu Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Patients must meet all the following criteria to be allowed to participate in clinical studies: 1. Patients with peripheral type IIIb and stage IV lung adenocarcinoma diagnosed by pathology or clinical examination, diameter of advanced lesion 4.0 × 10^9/L, PLT > 80 × 10^9/L; 8. Liver function: ALT and AST = 2 times ALT/AST normal value upper limit; 9. Kidney function: BUN and Cr = 1.5 times normal upper limit(ULN) or creatinine clearance = 60mL/min; 10. No other severe cardio-cerebrovascular diseases that affect treatment; 11. Patients agree to join the group and sign informed consent form.

Exclusion criteria

Exclusion criteria: Patients can not enter or continue research if they have one of the following conditions: 1. Women who are breastfeeding, pregnant or preparing for pregnancy; 2. Patients undergoing local treatment within the past four weeks; 3. Patients treated with chemotherapy or immunotherapy within the past four weeks; 4. Participants of other clinical trials within the past four weeks; 5. Patients known to be allergic to the composition of the test sample or its analogues; 6. Patients with cognitive dysfunction or have been judged by the researcher to have poor adherence to treatment; 7. Patients with contraindications of intratumoral injection with percutaneous lung puncture; 8. Other severe, acute or chronic diseases that may interfere with the interpretation of the results of the study and are judged by the researchers to be unsuitable for participation in clinical trials; 9. Those who are considered unsuitable for clinical trials.

Design outcomes

Primary

MeasureTime frame
Imaging evaluation of changes in lesion diameter;

Secondary

MeasureTime frame
Metabolism of target lesions;Immunization indicators;Tumor markers;quality of life;

Countries

China

Contacts

Public ContactYi Zhang

Xuanwu Hospital, Capital Medical University

steven9130@sina.com+86 13141370703

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026