Ignite Creation Date:
2024-10-26 @ 3:42 PM
Last Modification Date:
2024-10-26 @ 3:42 PM
Study NCT ID:
NCT06633120
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-09-25
Brief Title:
In Vitro Maturation of Human Eggs
Sponsor:
None
Organization:
None
Study Overview
Official Title:
In Vitro Maturation of Human Eggs
Status:
RECRUITING
Status Verified Date:
2024-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
CCRM Fertility a global pioneer in fertility treatment research and science is seeking participants for a new study on in vitro maturation IVM IVM requires less hormones to stimulate the ovaries than IVF making it more affordable than IVF with fewer side effects Participants that qualify for the study will receive a free cycle of IVM treatment at CCRM Fertility and including a new patient consultation fertility testing preimplantation genetic testing for aneuploidies PGT-A anesthesia and some medication
Detailed Description:
Patients will undergo a complete IVF workup to qualify for study Once passing their baseline appointment patients will undergo a three day low dose stimulation followed by egg retrieval 18-22 hours post last medication dosage Immature oocytes will be retrieved from the ovaries via ultrasound guided TV aspiration and matured overnight in the laboratory Mature oocytes will be fertilized via ICSI the following day and cultured to the blastocyst stage Biopsy of the first 14 blastocysts are included with this package patients have the option biopsy additional embryos if available Biopsies will be sent for PGTA testing This study also includes preparation for and the first frozen embryo transfer Some FET medication is included as well as testing through the first pregnancy test
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