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OpenTrials
Completed

NCT Number: NCT02764255

Embryoscope and Reproductive Outcome

cases with embyos cultured in the standard incubator and evaluated only by morphology are compared to cases with embryos continuously monitored by the embryoscope followed by embryo selection based on a multivariable model

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Key information

Conditions

Invitro Fertilization

Age range

18 year–39 year

Sex eligibility

Female

Study type

Observational

About this study

cases with embyos cultured in the standard incubator and evaluated only by morphology (control group) are compared to cases with embryos continuously monitored by the embryoscope followed by embryo selection based on a multivariable model(study group)

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient age:25-40 years old
  • BMI:18-30
  • patients with first or second ICSI trial

Exclusion criteria

  • AMH <1
  • severe male factor(total motile sperm <1 million)
  • frozen embryo transfer cycles
  • patients with endocrinopathies or thrombophilia
  • patients on medical treatment which may interfere with results
  • hydrosalpinx

Treatment and study plan

Primary outcomes

  1. clinical pregnancy rate

    Time frame: 14 days after embryo transfer

    transvaginal ultrasound done to assess the gestational sac

Sponsors and collaborators

Lead sponsor

Ahmed Maged

Other

Registry information

Official study title

Does Embryoscope Improve Reproductive Outcome in ICSI Patients

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
May 6, 2016
Registry last updated
Jul 25, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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