Viewing Study NCT00176644



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Last Modification Date: 2024-10-26 @ 9:16 AM
Study NCT ID: NCT00176644
Status: TERMINATED
Last Update Posted: 2023-09-13
First Post: 2005-09-13

Brief Title: Phase II Trial of Transdermal Estradiol for Hormone Refractory Prostate Cancer
Sponsor: University of Medicine and Dentistry of New Jersey
Organization: Rutgers The State University of New Jersey

Study Overview

Official Title: Phase II Trial of Transdermal Estradiol in Patients With Hormone Refractory Prostate Cancer
Status: TERMINATED
Status Verified Date: 2023-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Treatment ineffective
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Multiple trials have shown the efficacy of estrogen therapy in metastatic prostate cancer and most recently trials have supported the use of transdermal estrogens patch in the patient population with a decreased risk of cardiovascular disease as compared to the oral estrogens We plan to study the use of transdermal estrogen at a dose of 04mg qd We will evaluate the toxicities and measure quality of life We will assess PSA response and measurable disease response This will be a trial available to the Cancer Institute of New Jersey Oncology Group We will enroll a total of 33 patients We will plan to enroll 10 at CINJPatients will wear the patches 4 continuously We will obtain blood work and clinic evaluations every three weeks We will assess quality of life through a questionnaire given to patient every three weeks
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
P30CA072720 NIH Cancer Institute of New Jersey httpsreporternihgovquickSearchP30CA072720
CINJ 080419 OTHER None None