MedPath

Intrauterine Embryo Development With ANECOVA Device

Phase 3
Terminated
Conditions
Healthy
Registration Number
NCT00480103
Lead Sponsor
Instituto Valenciano de Infertilidad, IVI VALENCIA
Brief Summary

We aim to compare the morphological and chromosomal features of human embryos cultured In Vitro versus those developed in a new In Vivo culture system with encapsulation in utero as well as implantation and pregnancy rate.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • Women age below 37
  • Hormonal serum levels within normal ranges (FSH, LH, E2, PRL, P4, T4, TSH)
  • Negative serologic screening for HIV, Hep B and C
  • No uterine or ovarian alterations found by ultrasound
  • Normal BMI (19 - 29 kg/m2).
Exclusion Criteria
  • At least 8 stage MII oocytes are not retrieved
  • Endometriosis or PCO
  • Severe male factor in the partner

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Instituto Valenciano de Infertilidad Spain

🇪🇸

Valencia, Spain

© Copyright 2025. All Rights Reserved by MedPath