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Clinical Study in Treatment of Malignant Ascites of Ovarian Cancer With Intraperitoneal Injection Bevacizumab Combined With Intraperitoneal Hyperthermic Perfusion Chemotherapy

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01838538
Enrollment
54
Registered
2013-04-24
Start date
2011-06-30
Completion date
Unknown
Last updated
2013-04-24

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

Conditions

Ovarian Cancer With Malignant Ascites

Brief summary

To study the efficacy and safety of intraperitoneal injection bevacizumab combined with intraperitoneal hyperthermic perfusion chemotherapy in treatment of malignant ascites of ovarian cancer. To analyze the clinical significance of the concentration change of vascular endothelial growth factor (VEGF) in ascites in treatment of intraperitoneal injection bevacizumab

Interventions

DRUGBevacizumab
DRUGTC:paclitaxel + carboplatin

Sponsors

Chinese PLA General Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 75 Years

Inclusion criteria

* Signed informed consent obtained prior to initiation of any study-specific procedures and treatment as confirmation of the patient's awareness and willingness to comply with the study requirements. * Histologically confirmed and documented ovarian cancer with malignant ascites. * ECOG(Eastern Cooperative Oncology Group, ECOG) PS 0-2. * Life expectancy of \>3 months. * No serious inadequate bone marrow function, liver and renal function or significant cardiovascular disease.

Exclusion criteria

* Known hypersensitivity to any of the study drugs or excipients. * Any current anti-cancer therapy. * No evidence of ascites. * Key organ dysfunction. * Significant cardiovascular disease (e.g. congestive heart failure (CHF), uncontrolled cardiac arrhythmia, angina, heart valve disease, myocardial infarction and refractory hypertension need to be long time controlled by medicine). * Non-healing wound, ulcer or bone fracture. * Uncontrolled psychiatric history.

Design outcomes

Primary

MeasureTime frame
objective response rate24month

Countries

China

Contacts

Primary ContactNan Du, PhD
dunan05@yahoo.com.cn861068989123
Backup ContactJihua Chen, MD
jihua.chen@roche.com862128922576

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026