Clinical Trials Directory

Trials / Completed

CompletedNCT02793089

Risk of Ectopic Pregnancy and Variation of Luteal Estradiol and Progesterone Levels in IVF

Retrospective Cohort Study of Increased Risk of Ectopic Pregnancy Associated With Marked Variation of Estradiol During the Early Luteal Phase and High Progesterone on hCG Day in IVF

Status
Completed
Phase
Study type
Observational
Enrollment
578 (actual)
Sponsor
IVI Vigo · Academic / Other
Sex
Female
Age
25 Years – 45 Years
Healthy volunteers
Not accepted

Summary

This study evaluates the increased risk of ectopic pregnancy associated with marked variation of estradiol during the early luteal phase and high progesterone on hCG day in IVF.

Detailed description

This is a retrospective cohort study of 578 patients who had no risk of EP (672 fresh transfer IVF cycles) between January 2005 and December 2014. Few studies have reported the relation between hormonal levels and ectopic pregnancy (EP) in IVF. Investigators describe EP incidence according to estradiol (E2) and progesterone (P4) levels on hCG day and seven days later (hCG+7) or their variation between both days.

Conditions

Interventions

TypeNameDescription
OTHERAnalysis of Ectopic Pregnancy incidenceCollect retrospectively data. Analysis of Ectopic Pregnancy incidence through Estradiol (E2) and progesterone (P4) levels on hCG day and seven days later (hCG+7)

Timeline

Start date
2005-01-01
Primary completion
2016-05-01
Completion
2016-05-01
First posted
2016-06-08
Last updated
2016-06-08

Source: ClinicalTrials.gov record NCT02793089. Inclusion in this directory is not an endorsement.