Viewing Study NCT00600106



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Last Modification Date: 2024-10-26 @ 9:42 AM
Study NCT ID: NCT00600106
Status: COMPLETED
Last Update Posted: 2019-04-24
First Post: 2008-01-11

Brief Title: Data Analyses for Ancillary WISE Femhrt Hormone Replacement Study
Sponsor: Cedars-Sinai Medical Center
Organization: Cedars-Sinai Medical Center

Study Overview

Official Title: WISE Ancillary Study Data Analyses Efficacy of Hormone Replacement on Myocardial Ischemia in Postmenopausal Women With NormalMinimal Coronary Artery Disease Data Analysis
Status: COMPLETED
Status Verified Date: 2019-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of the main trial was to evaluate the effect of low dose hormone replacement therapy with 1 mg norethindrone10mcg ethinyl estradiol in postmenopausal women with a history of chest discomfort myocardial ischemia and no obstructive CAD For the purposes of this study as a core lab coordinating center the investigators will be performing P31 MRS core lab analyses hormone core lab analyses lipid core lab analyses glucose insulin and HOMA core lab analyses exercise stress testHolter monitor core lab analyses brachial artery reactivity test core lab analyses full study data analyses for manuscript preparation and the writing and submission and publication of manuscript

The main trial duration December 1999 - May 2003

The ancillary data analysis project duration April 2006 - March 2010
Detailed Description: See Brief Summary above

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
IRB0505140 OTHER University of Pittsburgh None