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Completed

NCT Number: NCT02593461

Diafert® for Embryo Selection and Fertility Improvement

Prospective, single-center, single-blind, randomized, controlled, two-arm, interventional study.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 3

Primary location

Centre D'Assistance Médicale À La Procréation

Schiltigheim, 67300, France

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Women at least 18 years old at the time of Informed Consent.
  • Able to understand and voluntarily sign an Informed Consent form approved by the relevant Independent Ethics Committee (IEC) governing the site.
  • First or second fresh Assisted Reproductive Technology (ART) cycle attempt (since last successful implantation, if any).
  • Eligible for elective SET of fresh embryo on Day 2/3. Elective SET is defined as a transfer for which there is more than one embryo in the same morphological ("best") category as that of the selected embryo.

Exclusion criteria

  • Presence or history of ovarian endometriotic cyst.
  • Presence or history of diagnosed severe endometriosis (i.e. stage IV of the revised American Fertility Society classification for endometriosis).
  • Hormonal, functional, anatomical and/or other abnormalities potentially increasing the risk of miscarriage and/or ectopic pregnancy as judged by the Investigator and determined by medical history and clinical laboratory. This includes, but is not limited to, uncontrolled diabetes mellitus, uncontrolled thyroid disease, alcoholism, drug abuse, abnormal uterine cavity etc.
  • History of two or more consecutive miscarriages.
  • Known history of human immunodeficiency virus, Hepatitis C virus and/or Hepatitis B virus infection.
  • The subject has other serious or acute conditions that, in the Investigator's opinion, would preclude her participation in the study.
  • Need for preimplantation genetic diagnosis/screening.
  • Use of time-lapse embryo imaging
  • Participating in oocyte donation procedure.
  • Participation in any interventional drug clinical investigation within 2 months
  • Dependency on sponsor or investigator (e.g. co-worker or family member).

Treatment and study plan

Daifert

Device

Control Group

Other

Other names: Control - Morphological Assessment

Primary outcomes

  1. Percentage of successful implantations

    Time frame: At Week 6

    The percentage of successful implantation 6 weeks after oocyte retrieval (±3 days), i.e. at approximately 8 weeks gestational age (±3 days) or 8 weeks of amenorrhea (± 3 days), in each group (Control and Interventional groups), overall and within each morphological embryo category, when elective Single Embryo Transfer (SET) is performed on Day 2 or 3.

    Successful implantation is defined as the presence in the uterus of at least one gestational sac with fetal heart activity identified on ultrasound.

Secondary outcomes

  1. Percentage of live births

    Time frame: Approximately Week 40 (pregnancy outcome)

    Percentage of live birth in the Control group and in the Interventional group when elective SET of a fresh embryo is performed on Day 2 or 3 after oocyte retrieval.

Sponsors and collaborators

Lead sponsor

Forest Laboratories

Industry

Registry information

Official study title

A Prospective, Single-center, Randomized, Two-arm, Interventional Study to Evaluate the Implantation Rate of Embryos Selected on the Basis of Morphology and Granulocyte-Colony Stimulating Factor (G-CSF) Concentration in the Ovarian Follicular Fluid (FF) - FF G-CSF - Compared to the Implantation Rate of Embryos Selected on the Basis of Morphology Alone When Elective Single Embryo Transfer (SET) of a Fresh Embryo is Performed on Day 2/3 After Oocyte Retrieval

Acronym: DESTINy

Important dates

Study start
2015
Primary completion
2016
Study completion
2017
First posted
Nov 2, 2015
Registry last updated
Aug 1, 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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