KIDScore D3 Clinical Study

Sponsor
Vitrolife (Industry)
Overall Status
Completed
CT.gov ID
NCT03740828
Collaborator
(none)
81
6
12.7
13.5
1.1

Study Details

Study Description

Brief Summary

The aim of this study is to demonstrate that the KIDScore D3 may be used to identify those embryos on Day 3 that are most likely to form blastocysts.

Condition or Disease Intervention/Treatment Phase
  • Device: KIDScore D3

Detailed Description

The safety and effectiveness of the KIDScore D3 was investigated in a prospective study. The study was performed as a single arm, multicenter clinical study conducted at six sites in the United States. This was a non-interventional clinical study where the KIDScore D3 was not used during patient treatment. Briefly, the purpose of the study was to collect data to evaluate the safety and effectiveness of the KIDScore D3's ability to predict which embryos are most likely to develop to blastocyst stage. This was evaluated by using the KIDScore D3 as adjunct information to traditional morphological grading. Imaging data was collected on embryos cultured to day 5. Embryologists were masked to imaging data and evaluation was only based on morphology and KIDScore D3 scores.

This study aims at analyzing the utilization of established morphology methods with adjunct outcome of an algorithm (KIDScore D3) that provides a score (1 - 5) from timings of morphokinetic events.

A double-blinded, multi-center study, designed to evaluate the odds ratios and other measures for outcomes of methodologies used for embryo assessment: day 3 morphology alone and day 3 morphology with KIDScore D3 results as adjunct information.

Study Design

Study Type:
Observational [Patient Registry]
Actual Enrollment :
81 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
KIDScore D3 Clinical Study
Actual Study Start Date :
Sep 20, 2016
Actual Primary Completion Date :
Oct 12, 2017
Actual Study Completion Date :
Oct 12, 2017

Arms and Interventions

Arm Intervention/Treatment
Women undergoing IVF treatment

Device: KIDScore D3 study

Device: KIDScore D3
Embryos are scored using the KIDScore D3 algorithm based on annotated morphokinetic parameters.

Outcome Measures

Primary Outcome Measures

  1. Prediction of blastocyst outcome [1-2 months]

    The primary endpoint of this study was to assess the association between the adjunct prediction using KIDScore D3 of blastocyst outcome and the actual blastocyst outcome. The Odds Ratio (OR) for the adjunct prediction of blastulation is required to be statistically significantly greater than 1, for good/fair embryos. This will demonstrate that adjunctive use of KIDScore D3 leads to embryologist predictions for Day 5 blastulation that is informative for blastocysts outcome.

Secondary Outcome Measures

  1. Embryo-Level Diagnostic Performance Measures [1-2 Months]

    The specificity was calculated for morphology alone prediction and compared to the specificity for adjunct prediction. Comparable calculations was done for sensitivity, negative predictive value, positive predictive value, negative likelihood ratio and positive likelihood ratio. The above measures were given both as an overall and for each panelist, assessing the performance measures without and with adjunct prediction.

  2. Top 2 Embryo Analysis [1-2 Months]

    This analysis included the top 2 embryos selected by each panelist based on morphology alone. The assessment of whether or not the OR is significantly greater than 1, was done by the use of a generalized linear mixed model (GLMM)

  3. Treatment Level Analyses [1-2 Months]

    For the performance assessments of treatment level analyses the predicted blastocyst outcome were compared with the actual blastocyst outcome with each treatment.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Women undergoing IVF treatment
Exclusion Criteria:
  • Less than 5 actively dividing embryos

Contacts and Locations

Locations

Site City State Country Postal Code
1 Fertility Specialists Medical Group, Inc San Diego California United States 92123
2 Laurel Fertility Care San Francisco California United States 94109
3 Pacific Fertility San Francisco California United States 94133
4 South Florida Institute Fro Reproductive Medicine Miami Florida United States 33143
5 Midwest Fertility Institute Carmel Indiana United States 46032
6 New York Fertility Institute New York New York United States 10028

Sponsors and Collaborators

  • Vitrolife

Investigators

  • Principal Investigator: Belinda Dueholm, MSc, Vitrolife A/S

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Vitrolife
ClinicalTrials.gov Identifier:
NCT03740828
Other Study ID Numbers:
  • FU1028_Clinical study
First Posted:
Nov 14, 2018
Last Update Posted:
Nov 14, 2018
Last Verified:
Nov 1, 2018
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Vitrolife
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 14, 2018