Viewing Study NCT00166478



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Last Modification Date: 2024-10-26 @ 9:15 AM
Study NCT ID: NCT00166478
Status: COMPLETED
Last Update Posted: 2010-01-28
First Post: 2005-09-12

Brief Title: Exisulind Prior to Radical Prostatectomy
Sponsor: Mayo Clinic
Organization: Mayo Clinic

Study Overview

Official Title: A Prospective Controlled Phase II Study of Preoperative Exisulind Therapy Initiated Prior to Radical Prostatectomy Effect on Apoptosis
Status: COMPLETED
Status Verified Date: 2010-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This trial will compare no treatment to exisulind therapy Patients enrolled on the treatment arm will begin treatment 4 weeks prior to the scheduled date of surgical removal of the prostate and will take 375 mg by mouth daily for the 4 weeks prior to radical prostatectomy Participants will be followed for total of 2 months from the time of starting study drug
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
N01-CN-75017 None None None