Skip to content

A randomized parallel controlled trial for different endocytosis administration and irinotecan in the treatment of malignant peritoneal effusion induced by recurrent ovarian cancer

A randomized parallel controlled trial for different endocytosis administration and irinotecan in the treatment of malignant peritoneal effusion induced by recurrent ovarian cancer

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018359
Enrollment
Unknown
Registered
2018-09-13
Start date
2019-01-01
Completion date
Unknown
Last updated
2018-09-17

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

Conditions

Malignant ascites caused by ovarian cancer

Interventions

Group 1:irinotecan single drug chemotherapy
Group 2:irinotecan iv chemotherapy plus endocytosis iv therapy
Group 3:Irinotecan iv chemotherapy plus endor peritoneal peritoneal perfusion therapy
Group 4:Irinotecan iv chemotherapy plus endor peritoneal peritoneal perfusion therapy

Sponsors

Liuzhou Worker's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) aged 18 to 75 years; (2) it was diagnosed as ovarian malignant tumor by histopathological/cytological examination, which recurred after initial treatment and was platinum-resistant ovarian cancer with cancerous ascites; (3) score of the eastern United States tumor cooperative group (ECOG) was 0-2; (4) the predicted survival period is not less than 2 months; (5) the main organs such as heart and lung function normally; (6) more than 4 weeks from major surgery; (7) entered the group voluntarily, signed the informed consent, followed well and cooperated with the follow-up

Exclusion criteria

Exclusion criteria: (1) uncontrolled central nervous system metastasis with intracranial hypertension; (2) tendency of bleeding, especially the occurrence of obvious gastrointestinal bleeding within the last 4 weeks, or receiving thrombolytic therapy or anticoagulation therapy; (3) used other research drugs within 30 days, or participated in other clinical studies at the same time; (4) had myocardial infarction within 6 months, or present unstable angina pectoris, cardiac insufficiency, and severe hepatic and renal insufficiency; (5) patients with severe chronic obstructive pulmonary disease and/or respiratory failure, severe intestinal adhesion, and intestinal obstruction; (6) there are serious uncontrolled infection.

Design outcomes

Primary

MeasureTime frame
Objective response rate;Blood CA125;bloodVEFG;

Secondary

MeasureTime frame
Time to progression;Time to progression;Quality of life;Functional status score KPS;

Countries

China

Contacts

Public ContactHe Hongying

Liuzhou Worker's Hospital

chensaiqiong1983@163.com+86 13607728346

Outcome results

None listed

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