Ignite Creation Date:
2024-07-17 @ 10:52 AM
Last Modification Date:
2024-10-26 @ 3:34 PM
Study NCT ID:
NCT06492785
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-07-10
First Post:
2024-07-01
Brief Title:
Hyaluronic Acid-enriched Transfer Medium in Single Blastocyst Transfer
Sponsor:
Northwest Womens and Childrens Hospital Xian Shaanxi
Organization:
Northwest Womens and Childrens Hospital Xian Shaanxi
Study Overview
Official Title:
Use of Hyaluronic Acid-enriched Transfer Medium in Women Undergoing Single Blastocyst Transfer a Multicenter Randomized Controlled Trial
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-07
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 is to compare the live birth rates of high concentration of Hyaluronic Acid 05 mgml transfer medium EmbryoGlue to those containing low Hyaluronic Acid concentrations 0125 mgml G2 medium in women undergoing single fresh and frozen blastocyst transfer
Detailed Description:
The single blastocyst-stage embryo transfer cycles will be randomised in a 11 allocation with block sizes of 2 and 4 on the day of Embryo Transfer ET This randomisation process will be centrally managed via a web-based electronic data capture system and will be stratified according to the treatment center The allocation sequence and the designated treatment will be completely concealed from the participating couples clinicians - including those conducting the transfer procedures - and outcome assessors Given the intrinsic viscous nature of EmbryoGlue embryologists who who are responsible for the procedures in the laboratory will not be subjected to blinding Only at the end of the study when data collection is completed the allocation sequence will be revealed to the primary investigators
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None