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Clinical efficacy of bevacizumab combined with cisplatin in the treatment of lung cancer-caused malignant pleural effusion and ascites

Clinical efficacy of bevacizumab combined with cisplatin in the treatment of lung cancer-caused malignant pleural effusion and ascites

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100048959
Enrollment
Unknown
Registered
2021-07-19
Start date
2018-05-31
Completion date
Unknown
Last updated
2022-03-28

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

Conditions

Pleural and ascites of lung cancer

Interventions

2 groups:Cisplatin combined with bevacizumab vs contral

Sponsors

BenQ Hospital Affiliated to Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: A total of 86 patients with malignant pleural and ascites caused by lung cancer admitted to our hospital from June 2018 to September 2020 were selected. Histologically or pathologically diagnosed as a lung cancer patient with clinical stage IV or above, the pleural effusion was confirmed to be malignant pleural effusion by exfoliated cytology and ultrasonography; the expected survival time is> 3 months and 1 patient before enrollment Has not received chemotherapy, targeted therapy or other anti-tumor treatments for the first month; routine blood tests, liver function, renal function, and electrocardiogram examinations were performed before treatment, and there were no abnormalities; none of the patients had a history of allergy to biological agents

Exclusion criteria

Exclusion criteria: Received chemotherapy and targeted therapy within the past month; patients with severe cardiovascular and liver and kidney dysfunction; patients with allergic reactions to the drugs used in this study (cisplatin, bevacizumab, etc.); pregnant and lactating women .

Design outcomes

Primary

MeasureTime frame
Quality of life score;

Secondary

MeasureTime frame
(Hypoxia inducible factor, HIF- 1a;Pleural fluid and ascites relief index;

Countries

China

Contacts

Public ContactZhou Zhi

BenQ Hospital Affiliated to Nanjing Medical University

zhouzhi9419@Hotmail.com+86 13813017503

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 14, 2026