Study of Bevacizumab Followed by Bevacizumab Consolidation for Ovarian Cancer
Completed · Phase 2
Conditions studied: Advanced Ovarian Carcinoma, Primary Peritoneal Carcinoma, Ovarian Carcinosarcoma
In brief
The purpose of this study is to evaluate the tolerability of intraperitoneal cisplatin with intravenous paclitaxel and Avastin as defined by the proportion of patients able to complete 6 cycles of treatment.
Key facts
- Study ID
- NCT00511992
- Run by
- University of Oklahoma
- People needed
- 20
- Starts
- 2007-07-01
- Expected to finish
- 2015-08-03
- Last updated by the study team
- 2017-07-02
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Patients with stage II and III epithelial ovarian carcinoma, primary peritoneal carcinoma, or ovarian carcinosarcoma.
- Adequate bone marrow, renal, and hepatic function
- Patients must be entered no more than twelve weeks postoperatively
You may not qualify if…
- Patients with epithelial ovarian carcinoma of low malignant potential (borderline carcinomas).
- Stage IV or suboptimally debulked disease following primary cytoreductive surgery
- Patients who have received prior radiotherapy or chemotherapy.
Where it is running
- University of Oklahoma Health Sciences Center — Oklahoma City, Oklahoma, United States
Full record on ClinicalTrials.gov
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