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Comparison Of The Embryoscope Time-Lapse System With Standard Embryo Culture

Primary Purpose

Infertility

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Embryoscope Time Lapse System
Standard Embryo Culture
Sponsored by
Center for Human Reproduction
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infertility focused on measuring Infertility, Embryo Culture, Laboratory Technique

Eligibility Criteria

18 Years - 48 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Patients already planning to undergo in vitro fertilization

Exclusion Criteria:

  • Patients with more than 12 oocytes will be excluded from this trial

Sites / Locations

  • Center for Human Reproduction

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Embryoscope Time Lapse System

Standard Embryo Culture

Arm Description

All embryos from patients randomized to this arm will be cultured in the Embryoscope culture system from the time of insemination until the time of transfer on day 3. All staff interaction with the embryos or with maintenance or supervision of the system will be timed.

All embryos from patients randomized to this arm will be cultured in the standard embryo culture system from the time of insemination until the time of transfer on day 3. All staff interaction with the embryos or with maintenance or supervision of the system will be timed.

Outcomes

Primary Outcome Measures

Personnel Effort
Number of minutes spent by laboratory personnel technical staff in support of each system

Secondary Outcome Measures

Embryo Quality
Number of Grade A best quality of day 3 embryos (based on cell number and degree of fragmentation)

Full Information

First Posted
September 18, 2014
Last Updated
April 18, 2018
Sponsor
Center for Human Reproduction
Collaborators
FertiliTech Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT02246309
Brief Title
Comparison Of The Embryoscope Time-Lapse System With Standard Embryo Culture
Official Title
Comparison Of The Embryoscope Time-Lapse System With Standard Embryo Culture at Center for Human Reproduction(CHR):an Open Label Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2015
Overall Recruitment Status
Terminated
Why Stopped
Equipment was loaned Lifglobal, Guilford, CT, USA and had to be returned.
Study Start Date
September 2014 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Center for Human Reproduction
Collaborators
FertiliTech Inc.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
"Embryoscopes," allow for embryo culture to be performed in an automated incubation system under time lapse photography. Manufacturers of these systems (and investigators who have used these systems) claim that the availability of 24-hour time-lapse photographic control improves embryo selection and, therefore, IVF (in vtro fertilization) pregnancy rates. They also claim that use of this system saves laboratory personnel time. This study will randomize approximately 120 patients (60 in each arm) to standard embryo culture or to culture in an Embryoscope. The primary endpoint will be a comparison of time spent by the laboratory personnel with each system. Secondary endpoints will be IVF outcomes.
Detailed Description
A large number of IVF centers all around the world are converting from standard embryology practice, where embryos are by embryologists manually processed during culture, to so-called "embryoscopes," where embryo culture is performed in an automated incubation system under time lapse photography. Manufacturers of these systems (and investigators who have used these systems) claim that the availability of 24-hour time-lapse photographic control improves embryo selection and, therefore, IVF pregnancy rates. They also claim that use of this system saves laboratory personnel time. The FDA has so far, therefore, approved for sale at least 2 such systems In the USA. (i) Our analysis of the published literature has failed to find studies in support of the claim that utilization of such equipment really improves pregnancy rates with IVF; and (ii) Investigators are concerned that CHR's highly adversely selected patient population may demonstrate different utilization outcomes from standard patient populations, especially since this equipment is usually utilized to culture embryos to blastocyst stage (days 5/6), while CHR cultures most patients only to day-3. Investigators, therefore, contacted the manufacturer of the first FDA approved system, and explained our concerns. The manufacturer agreed to loan us one of their systems for a 4-months long study free of charge (CHR just pays a nominal amount for installation and training costs) but will be financially responsible for supplies. During these 4 months, CHR will perform an open-label prospective (registered) and randomized clinical trial, in which investigators, based on computerized randomization, will assign all CHR patients (who agree to participate with informed written consent), either to standard embryology or "embryoscope" embryology. Recruiting approximately 30 patients per month into the study is anticipated, which would give us a population of ~n=60 in each study group. Patient with excessive numbers of eggs retrieved (>12) will be excluded since the purpose of this study is to investigate the utility of the system in a relatively adversely selected patient population. All other patients will be offered participation. The study will have as primary end point a time analysis of laboratory manpower, under which the time spent on each patient by embryologist will be recorded and compared and as secondary end point IVF cycle outcome, defined by number of good quality embryos available for transfer, implantation rates and clinical pregnancy rates.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility
Keywords
Infertility, Embryo Culture, Laboratory Technique

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
31 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Embryoscope Time Lapse System
Arm Type
Experimental
Arm Description
All embryos from patients randomized to this arm will be cultured in the Embryoscope culture system from the time of insemination until the time of transfer on day 3. All staff interaction with the embryos or with maintenance or supervision of the system will be timed.
Arm Title
Standard Embryo Culture
Arm Type
Active Comparator
Arm Description
All embryos from patients randomized to this arm will be cultured in the standard embryo culture system from the time of insemination until the time of transfer on day 3. All staff interaction with the embryos or with maintenance or supervision of the system will be timed.
Intervention Type
Device
Intervention Name(s)
Embryoscope Time Lapse System
Intervention Description
The EmbryoScope® time-lapse system is a unique platform facilitating improved IVF treatment, flexible work routines and effective communication, through comprehensive documentation of embryo development and evolving improvements in selection.
Intervention Type
Device
Intervention Name(s)
Standard Embryo Culture
Other Intervention Name(s)
Standard water jacketed incubator system
Intervention Description
Standard embryo culture in a Standard water jacketed carbon dioxide/low oxygen incubator system.
Primary Outcome Measure Information:
Title
Personnel Effort
Description
Number of minutes spent by laboratory personnel technical staff in support of each system
Time Frame
Three days
Secondary Outcome Measure Information:
Title
Embryo Quality
Description
Number of Grade A best quality of day 3 embryos (based on cell number and degree of fragmentation)
Time Frame
Three Days
Other Pre-specified Outcome Measures:
Title
Clinical Pregnancy Rate
Description
Existence of Clinical Pregnancy documented by sonogram 4 weeks after embryo transfer
Time Frame
4 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
48 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients already planning to undergo in vitro fertilization Exclusion Criteria: Patients with more than 12 oocytes will be excluded from this trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David Barad, MD
Organizational Affiliation
Center for Human Reproduction
Official's Role
Principal Investigator
Facility Information:
Facility Name
Center for Human Reproduction
City
New York
State/Province
New York
ZIP/Postal Code
10021
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
27553622
Citation
Wu YG, Lazzaroni-Tealdi E, Wang Q, Zhang L, Barad DH, Kushnir VA, Darmon SK, Albertini DF, Gleicher N. Different effectiveness of closed embryo culture system with time-lapse imaging (EmbryoScope(TM)) in comparison to standard manual embryology in good and poor prognosis patients: a prospectively randomized pilot study. Reprod Biol Endocrinol. 2016 Aug 24;14(1):49. doi: 10.1186/s12958-016-0181-x.
Results Reference
result

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Comparison Of The Embryoscope Time-Lapse System With Standard Embryo Culture

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