Actively Recruiting
The Impact of Personalized Prognostic Counseling on IVF Patient's Experience and Treatment Utilization
Led by Ginefiv · Updated on 2024-08-22
366
Participants Needed
2
Research Sites
101 weeks
Total Duration
On this page
Sponsors
G
Ginefiv
Lead Sponsor
U
Univfy Inc.
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study will be conducted in two phases. In the first phase, research subjects will be assigned to receive standard counseling. In the second phase, research subjects will receive Univfy counseling.
CONDITIONS
Official Title
The Impact of Personalized Prognostic Counseling on IVF Patient's Experience and Treatment Utilization
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged between 18 and 43 years
- Healthcare providers have determined that IVF treatment using the patient's own eggs is indicated
You will not qualify if you...
- Patients who are part of same-sex couples
- Patients undergoing DuoStim and/or PGT-M/-SR
- Patients considering egg freezing instead of IVF
- Patients considering the use of donor eggs or gestational carrier
- Patients who are perimenopausal or menopausal
- Patients with very poor past IVF results including extremely poor oocyte or embryo quality, no embryos to transfer, no euploid embryos on PGT-A, or no blastocysts in extended culture
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Ginefiv S.L
Barcelona, Spain, 08015
Actively Recruiting
2
Ginefiv S.L
Madrid, Spain, 28018
Actively Recruiting
Research Team
X
Xinxin L Miao
CONTACT
J
Joaquín Llácer
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
SEQUENTIAL
Primary Purpose
OTHER
Number of Arms
2
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