Ovarian Cancer Clinical Trial

Feasibility Trial of Intraperitoneal Chemotherapy for Ovarian, Fallopian Tube, and Primary Peritoneal Carcinoma

Summary

The purpose of this study is to evaluate giving chemotherapy drugs directly into the abdomen (belly) along with intravenous administration.

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Full Description

Giving chemotherapy directly into the abdomen is called intraperitoneal (IP) chemotherapy. Because ovarian, fallopian, primary peritoneal and uterine cancer spread in the abdominal cavity, giving chemotherapy drugs by infusion into the abdominal cavity may result in a greater dose of the drugs reaching the tumor cells. Intraperitoneal treatments will be administered through an implantable peritoneal catheter. These catheters are to be inserted into the peritoneal cavity, tunneled through the subcutaneous tissue, and connected to an implantable port, which is placed in the subcutaneous tissue of the anterior, inferior thorax.

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Eligibility Criteria

Inclusion Criteria:

Patients with stage IA, IB, IC, II, III, IV and recurrent platinum sensitive epithelial ovarian carcinoma, fallopian tube carcinoma, primary peritoneal carcinoma, or ovarian carcinosarcoma. Histologic subtypes which are eligible include serous adenocarcinoma, endometrioid adenocarcinoma, mucinous adenocarcinoma, undifferentiated carcinoma, clear cell adenocarcinoma, mixed epithelial carcinoma, transitional cell carcinoma, malignant Brenner's tumor, adenocarcinoma (not otherwise specified), and carcinosarcoma.
Patients with advanced endometrial carcinoma, of any histology, including endometrioid adenocarcinoma, clear cell adenocarcinoma, and serous papillary carcinoma.
Patients with uterine carcinosarcoma of any stage are eligible.

Exclusion Criteria:

Patients with epithelial ovarian carcinoma of low malignant potential (borderline carcinomas).
Patients with septicemia, severe infection, or acute hepatitis.
Patients with prior malignancy or cancer treatment within the last five years.

Study is for people with:

Ovarian Cancer

Phase:

Phase 2

Estimated Enrollment:

21

Study ID:

NCT00582205

Recruitment Status:

Terminated

Sponsor:

University of Oklahoma

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There is 1 Location for this study

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University of Oklahoma Health Sciences Center
Oklahoma City Oklahoma, 73104, United States

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Study is for people with:

Ovarian Cancer

Phase:

Phase 2

Estimated Enrollment:

21

Study ID:

NCT00582205

Recruitment Status:

Terminated

Sponsor:


University of Oklahoma

How clear is this clinincal trial information?

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