Skip to content

Prospective clinical trial of autologous erythrocyte derived microparticles encapsulated methotrexate in the treatment of non-small cell lung cancer

Prospective clinical trial of autologous erythrocyte derived microparticles encapsulated methotrexate in the treatment of non-small cell lung cancer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-17012168
Enrollment
Unknown
Registered
2017-08-02
Start date
2017-08-10
Completion date
Unknown
Last updated
2017-08-21

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

Conditions

lung cancer

Interventions

erythrocyte-derived microparticles encapsulated methotrexate :erythrocyte-derived microparticles encapsulated methotrexate

Sponsors

Xiangyang Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Newly diagnosed as lung cancer; 2. Stable vital sign with Karnofsky index (KPS - Karnofsky Performance Status) more than 70; 3. Aged 18-75 years old; 4. Normal bone marrow hematopoietic function, no bleeding, blood routine: HGB >=90g/L, WBC >4.0*10^9/L; (NEU>=1.5*10^9/L), PLT>=100*10^9/L; 5. Liver function: total bilirubin <=1.5ULN; AST?ALT<=2.5ULN; Alkaline phosphatase<=1.5ULN; 6. BUN within 1.5 time upper limit of normal; Creatinine clearance rate more than 50mL/min; 7. Normal ECG, normal blood sugar levels; no other severe cardiopulmonary diseases 8. Agreed to participate in the study and sign an informed consent; 9. Without other severe comorbidities.

Exclusion criteria

Exclusion criteria: 1. Without pathological diagnosis; 2. Pregnant or lactating patients; 3. Allergy to multiple drugs; 4. With other severe comorbidities or psychological diseases; 5. Severe infection; 6. HIV positive; Treponema pallidum antibody positive;HCV positive;HBV positive; 7. Cognitive dysfunction; 8. Participation in other clinical trials within the recent four weeks; 9. Not available to participate in this clinical trials.

Design outcomes

Primary

MeasureTime frame
KPS;PS;Tumor volume;

Countries

China

Contacts

Public ContactTeinan Yi

Xiangyang Central Hospital

1721905183@qq.com+86 13871658799

Outcome results

None listed

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