Viewing Study NCT01257802



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Last Modification Date: 2024-10-26 @ 10:29 AM
Study NCT ID: NCT01257802
Status: TERMINATED
Last Update Posted: 2017-06-27
First Post: 2010-12-09

Brief Title: GnRH-a for Ovarian Protection During CYC Therapy for Rheumatic Diseases
Sponsor: Joseph Mccune
Organization: University of Michigan

Study Overview

Official Title: GnRH-a for Ovarian Protection During CYC Therapy for Rheumatic Diseases
Status: TERMINATED
Status Verified Date: 2017-05
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: LUPRON
Brief Summary: The purpose of this study it to determine whether the use of a gonadotropin releasing hormone GnRH-agonist depot-leuprolide acetate during cyclophosphamide CYC therapy in women with rheumatic diseases will provide greater ovarian protection than placebo
Detailed Description: Patients will be women ages 18-40 with either a severe rheumatic disease requiring cyclophosphamide or interstitial lung disease requiring cyclophosphamide to be administered either daily orally monthly intravenously or intravenously every 2 weeks for 6 doses Because cyclophosphamide treatment may be required urgently for some indications study entry may occur before either the first or second dose of cyclophosphamide for patients receiving cyclophosphamide intravenously

Of 16 participants who were screened only 14 were randomized and only 7 participants actually completed the study Due to this low number follicle stimulating hormone FSH levels were not obtained

Secondary outcome measures that are not available include presence of menses and FSH

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
5R01HD066139 NIH None httpsreporternihgovquickSearch5R01HD066139