Viewing Study NCT00120549



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Last Modification Date: 2024-10-26 @ 9:12 AM
Study NCT ID: NCT00120549
Status: COMPLETED
Last Update Posted: 2005-07-19
First Post: 2005-07-11

Brief Title: Study of Assisted Hatching of Cleavage Stage Embryos
Sponsor: Shady Grove Fertility Reproductive Science Center
Organization: Shady Grove Fertility Reproductive Science Center

Study Overview

Official Title: Prospective Randomized Trial of Assisted Hatching of Cleavage Stage Embryos
Status: COMPLETED
Status Verified Date: 2005-07
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 purpose of this study was to determine if assisted embryo hatching can improve pregnancy rates for good prognosis patients undergoing in vitro fertilization IVF with day 3 embryo transfer
Detailed Description: Assisted hatching is a procedure in which a hole is made in the hard covering of a developing embryo to allow the embryo to hatch more easily from this shell This procedure is sometimes used before transferring embryos to patients after in vitro fertilization IVF in an attempt to improve resulting pregnancy rates Assisted hatching has been shown to improve outcomes among certain groups of patients such as older patients or patients with a history of IVF treatment and embryo transfer without success Whether this procedure could benefit the broader patient population remains unclear The purpose of this study was to evaluate potential benefits of assisted hatching for good prognosis patients who would not typically be treated with assisted hatching under current standard protocols Pregnancy rates were compared between good prognosis patients undergoing IVF with day-3 embryo transfer with or without assisted hatching of the transferred embryos

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