Ignite Creation Date:
2024-05-05 @ 4:53 PM
Last Modification Date:
2024-10-26 @ 9:25 AM
Study NCT ID:
NCT00334243
Status:
TERMINATED
Last Update Posted:
2011-10-06
First Post:
2006-06-06
Brief Title:
Protocols for Improved in Vitro Fertilization IVF Outcomes
Sponsor:
University of California San Francisco
Organization:
University of California San Francisco
Study Overview
Official Title:
Protocol Evaluation for Improved In Vitro Fertilization Outcomes
Status:
TERMINATED
Status Verified Date:
2011-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
stopped due to limited enrollment 2 subjects were enrolled There was NO enrollment after November 2007
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Many infertile patients have a decreased chance of becoming pregnant when using in vitro fertilization IVF For these patients many different treatments are available but none of them have been shown to be better than the others We are testing which of three different treatments are better than the others Patients who are expected to have a decreased response to ovarian stimulation will be randomized to either a microflare protocol an antagonist protocol or a demi-halt protocol
Detailed Description:
Infertile patients with an anticipated poor response to ovarian stimulation will be randomized to one of three different protocols in their upcoming IVF cycle Each of the protocols will be performed as is the standard of care with the addition of serum evaluation during the course of the stimulation as well as follicular fluid analysis which is obtained as a byproduct of the oocyte retrieval Chart review will be performed to collect background characteristics including age ethnicity previous fertility treatment treatment response such as oocyte number embryo grade embryo quality and pregnancy outcome such as miscarriage singleton pregnancy or higher-order multiple pregnancy Statistical analysis will be performed to determine if one protocol leads to higher pregnancy rates and multivariate analysis will be performed to determine potential etiologic variables
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