Integrated Dose Escalation for Advanced, Localized Gynecologic Cancer (The IDEAL - GYN Trial)



Status:Active, not recruiting
Conditions:Cervical Cancer, Cancer, Women's Studies
Therapuetic Areas:Oncology, Reproductive
Healthy:No
Age Range:18 - Any
Updated:10/24/2018
Start Date:June 2012
End Date:June 2020

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The purpose of this study is to determine the maximum tolerated dose of integrated boost
radiation therapy when given with concurrent chemotherapy (cisplatin).


Inclusion Criteria:

- Biopsy confirmed malignancy of the gynecologic tract

- Involved pelvic or para-aortic lymph nodes

- Treatment plan to include delivery of concurrent chemoradiotherapy.

- Good performance status

- Negative pregnancy test in women of child-bearing potential

- Signed study-specific informed consent

- Lab results within study specific limits

Exclusion Criteria:

- Prior radiation to the abdomen or pelvis

- A history of Scleroderma or Inflammatory bowel disease

- Contraindication to chemotherapy or radiation
We found this trial at
1
site
Durham, North Carolina 27710
Principal Investigator: Junzo Chino, MD
Phone: 919-668-7336
?
mi
from
Durham, NC
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