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The prospective, single-arm open, multi-center Phase IV clinical study of the safety and effectiveness of chemotherapy regimens Lobaplatin- contained for Small cell lung cancer

The prospective, single-arm open, multi-center Phase IV clinical study of the safety and effectiveness of chemotherapy regimens Lobaplatin- contained for Small cell lung cancer

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-13003471
Enrollment
Unknown
Registered
2013-08-09
Start date
2013-08-19
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Small cell lung cancer

Interventions

Small cell lung cancer:chemotherapy regimens Lobaplatin-contained

Sponsors

Jilin Province Tumor Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Not less than 18 years old, male or female patients; 2. With the diagnosis of Small cell lung cancer confirmed by pathological or cytology tests; 3. Without limiting the phase and the once treatment; 4. With measurable tumor foci; 5. ECOG PS0-2; 6. Life expectancy >=3 months; 7. Laboratory parameters: Bone marrow function: ANC>=1.5×10^9/L; PLT>=100×10^9/L; HB>=90g/L; Hepatic function: STB and CB=60 ml/min (Cockcroft-Gault); 8. Keep contraception during the administration and 6 months later;not breastfeeding; 9. Voluntary to participate and sign informed consent document.

Exclusion criteria

Exclusion criteria: 1. Allergic to platinum drugs used in the trial; 2. The patients with coagulation dysfunction; 3. Other patients that are not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
the Safety;

Secondary

MeasureTime frame
the effectivenes;

Countries

China

Contacts

Public ContactYing Cheng
chengying@csco.org.cn+86 0431-85871236

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 25, 2026