Clinical Trials Directory

Trials / Terminated

TerminatedNCT01882166

Time-lapse Monitoring of Early Embryo Development After Ovarian Stimulation During Infertility Treatment

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
St. Olavs Hospital · Academic / Other
Sex
Female
Age
18 Years – 38 Years
Healthy volunteers
Not accepted

Summary

The number of children conceived by assisted reproductive technology is increasing in Nordic countries as well as worldwide. An important factor of success in treatment of infertility is a short "time to pregnancy" with impact on both economical aspects for the society and medical and psychological aspects for the couple. During treatment, success relies on 1) optimal stimulation of growth and maturation of multiple follicles by administration of exogenous follicle stimulating hormone (FSH), and 2) selection of the fertilized egg / embryo with the highest potential of implantation to be transferred to the mother. In the present project stimulation of egg production by human urine derived FSH (Fostimon®) and recombinant FSH (Puregon®) will be compared. To this end early embryo development and kinetics after fertilization will be evaluated. The system to be used is time-lapse recording of embryo morphology during the first days of embryo development by means of an embryoscope. Aim of this study is to investigate if Puregon and urinary Fostimon have different effect on embryo quality. The hypothesis of the study is that stimulation of egg production by these two types of follicle stimulating hormone does not have the same effect on early embryo quality.

Conditions

Interventions

TypeNameDescription
DRUGfostimon
DRUGpuregon

Timeline

Start date
2013-10-01
Primary completion
2015-01-01
Completion
2015-01-01
First posted
2013-06-20
Last updated
2018-09-14

Locations

1 site across 1 country: Norway

Source: ClinicalTrials.gov record NCT01882166. Inclusion in this directory is not an endorsement.