Viewing Study NCT00225433



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Last Modification Date: 2024-10-26 @ 9:19 AM
Study NCT ID: NCT00225433
Status: COMPLETED
Last Update Posted: 2015-12-03
First Post: 2005-09-21

Brief Title: Luteal Phase FSH in the IVF Poor Responder
Sponsor: University of Pennsylvania
Organization: University of Pennsylvania

Study Overview

Official Title: Luteal Phase Recombinant FSH vs Follicular Phase Recombinant FSH for IVF Stimulation in the Poor Responder
Status: COMPLETED
Status Verified Date: 2015-12
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: In vitro fertilization IVF is a common procedure used to assist couples who have difficulty conceiving a pregnancy IVF is a process where oocytes eggs are retrieved from a womans ovaries and fertilized with sperm in the laboratory In order to maximize the number of oocytes that can be retrieved a women undergoes ovarian stimulation with recombinant follicle stimulating hormone FSH Typically 6-20 oocytes are retrieved but in some cases there is a limited response to the stimulation producing a limited number of oocytes This is called poor ovarian response

This study is designed to objectively compare two treatment regimens currently advocated in clinical practice but never compared directly The purpose is to assess ovarian response to starting treatment at the end of the preceding cycle may increase the number of developing oocytes
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
RRU013 None None None