Viewing Study NCT06471140



Ignite Creation Date: 2024-07-17 @ 11:40 AM
Last Modification Date: 2024-10-26 @ 3:32 PM
Study NCT ID: NCT06471140
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-06-24
First Post: 2024-06-18

Brief Title: Maternal Cardiovascular Adaption to Pregnancy in IVF Patients Following Frozen Embryo Transfer FET
Sponsor: Aalborg University Hospital
Organization: Aalborg University Hospital

Study Overview

Official Title: MRI Evaluation of Maternal Cardiovascular Response to Pregnancy in IVF Women Following Autologous Natural Cycle FET Programmed FET and After Donor Embryo Transfer
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-08
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: Aim of the study is to explore the effect of a lacking corpus luteum on maternal cardiovascular and metabolic adaption to pregnancy by the use of magnetic resonance imaging MRI
Detailed Description: The use of programmed frozen embryo transfer cycle FET in IVF women is associated with an increased risk of obstetric complications pregnancy-induced hypertension preeclampsia postpartum hemorrhage and placenta accreta compared to FET in natural cycle

The lack of corpus luteum in programmed cycles and the subsequent absence of circulating vasoactive substances may lead to an impaired cardio-vascular adaption to pregnancy and thereby an increased risk of pregnancy-induced hypertension and preeclampsia

The cardiovascular and metabolic adaption to pregnancy is evaluated throughout pregnancy by use of Magnetic Resonance Imaging MRI as well as non-invasive measurements by use of elastography and seismocardiography

Patients are screened for preeclampsia throughout pregnancy with measurements of blood pressure urine samples as well as blood samples

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