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A Single-arm Study to Evaluate the Efficacy and Safety of Intrapleural Combination Therapy with Lobaplatin and Erythromycin for Lung Cancer Mediated Malignant Pleural Effusion

A Single-arm Study to Evaluate the Efficacy and Safety of Intrapleural Combination Therapy with Lobaplatin and Erythromycin for Lung Cancer Mediated Malignant Pleural Effusion

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-14005452
Enrollment
Unknown
Registered
2014-11-06
Start date
2014-11-20
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

Lung cancer mediated malignant pleural effusion

Interventions

None listed

Sponsors

Shandong University, School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Advanced lung cancer confirmed histologically or pathologically; 2. Ultrasonography or CT scan showing plural effusion and malignant tumor cells found in the pleural fluid; 3. To be aged older than 18 years; 4. All subjects or their guardians must sign an informed consent before entering the trial.

Exclusion criteria

Exclusion criteria: 1. Lung cancer patients with indications for surgery; 2. Patients with thrombocytopenia or coagulation disorders; 3. Major organ dysfunction, such as heart,liver, kidney or lung; 4. Under current treatment with targeted agents; 5. Are allergic to lobaplatin or erythromycin.

Design outcomes

Primary

MeasureTime frame
Total efficiency (The total efficiency was calculated by taking the sum of CR+PR);

Secondary

MeasureTime frame
Progression free survival (PFS);Objective response rate (ORR);Overall survival (OS);Qualify of Life was evaluated by the Kanofsky score (KPS);Level of chronic dyspnea will be assessed using modified Medical Research Council dyspnea scale (MMRC);Adverse events (AEs);

Countries

China

Contacts

Public ContactLi Yu
qlliyu@163.com+86 13791122770

Outcome results

None listed

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