ChemoFx® PRO - A Post-Market Data Collection Study

Stopped early

Conditions studied: Ovarian Cancer, Fallopian Tube Cancer, Peritoneal Cancer, Uterine Neoplasms, Endometrial Cancer, Vaginal Cancer, Vulvar Cancer, Cervical Cancer

In brief

This study will collect patient demographic, oncology history, and physician reported outcome information following the initial round of chemotherapy received after a commercial ChemoFx® Final Report for the generation of hypotheses of potential patient cohorts for further sub-studies.

Key facts

Study ID

NCT00669422

Run by

Precision Therapeutics

People needed

2756

Starts

2006-10-01

Expected to finish

2012-10-01

Last updated by the study team

2012-10-05

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Patient has been diagnosed with a solid tumor malignancy and their physician has received a final report for ChemoFx® after August 1, 2006
• Chemotherapy must be clinically indicated for treatment of the patient's qualifying disease
• Patient must be at least 18 years of age
• Patient must have signed an IRB approved informed consent form for the data collection study prior to entry of data into the enrollment form in the database.

You may not qualify if…

• Patient pathology shows benign pathology for sample submitted
• Patient is not indicated to receive chemotherapy for their disease

Where it is running

• University of South Alabama — Mobile, Alabama, United States
• University of California San Francisco — San Francisco, California, United States
• Women's Cancer Center of Southern California — Sherman Oaks, California, United States
• GOA Torrance Memorial — Torrance, California, United States
• Hartford Hospital — Hartford, Connecticut, United States
• Yale University — New Haven, Connecticut, United States
• South Florida Center for Gynecologic Oncology — Boca Raton, Florida, United States
• West Coast Gynecologic Oncology — Clearwater, Florida, United States
• Florida Center for Gynecologic Oncology — Coconut Creek, Florida, United States
• Comprehensive Gynecologic Oncology — Delray Beach, Florida, United States
• Caruso and Gates MDs PA — Fort Lauderdale, Florida, United States
• Florida Gynecologic Oncology — Fort Myers, Florida, United States
• Gynecologic Oncology Associates — Hollywood, Florida, United States
• Sarasota Memorial Hospital — Sarasota, Florida, United States
• South Miami Gynecologic Oncology Group — South Miami, Florida, United States
• Palm Beach Cancer Institute — West Palm Beach, Florida, United States
• Southeastern Gynecologic Oncology, LLC — Riverdale, Georgia, United States
• Memorial Health University Medical Center — Savannah, Georgia, United States
• The Queens' Medical Center — Honolulu, Hawaii, United States
• Rush University — Chicago, Illinois, United States
• NorthShore Medical Group — Evanston, Illinois, United States
• Indiana University — Indianapolis, Indiana, United States
• Women's Cancer Center — Covington, Louisiana, United States
• CHRISTUS Schumpert Health System — Shreveport, Louisiana, United States
• University of Alabama at Birmingham — Birmingham, Alabama, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.