Viewing Study NCT06551376



Ignite Creation Date: 2024-10-26 @ 3:37 PM
Last Modification Date: 2024-10-26 @ 3:37 PM
Study NCT ID: NCT06551376
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-08-09

Brief Title: LATE LUTEAL PHASE VS CONVENTIONAL EARLY FOLLICULAR PHASE START IN IVF
Sponsor: None
Organization: None

Study Overview

Official Title: IVF CYCLE SCHEDULING WITH LATE LUTEAL PHASE VS CONVENTIONAL EARLY FOLLICULAR PHASE START TO AVOID WEEKENDS RETRIEVALS PROOF OF CONCEPT
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-08
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: To compare cycle outcomes after scheduling with the standard early follicular phase EFP versus late luteal phase LLP in patients undergoing GnRH antagonist cycles
Detailed Description: Objective To compare cycle outcomes after scheduling with the standard early follicular phase EFP versus late luteal phase LLP in patients undergoing GnRH antagonist cycles

Design Multicentric prospective non-randomized study

Setting Two university-affiliated private assisted reproduction centers

Patients Regularly cycling women aged 40 years with fewer than one previous IVF attempts were enrolled Previous low responses to controlled ovarian hyperstimulation ovarian surgery or polycystic ovary were exclusion criteria

Interventions Twenty patients started controlled ovarian stimulation COS after spontaneous menses similarly twenty patients started stimulation on the Friday previous to a spontaneous menses at the end of late luteal phase regardless of cycle day

Main Outcome Measures Primary outcome number of mature oocytes retrieved Secondary outcomes fertilization rate viable embryo rate per oocyte retrieved cancellation rate and clinical pregnancy outcomes from FET cycles

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