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Improvement of Cell Selection in Reproductive Techniques

Primary Purpose

Infertility

Status
Unknown status
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Z-Score and computer algorithm
Z-Score
Sponsored by
Jürgen Weiss
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infertility focused on measuring Assisted reproductive technology (ART), zygotes, Z-score (Zygote Score), Infertility

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria (for both male and female, couples):

  • Woman with age 18 years or older
  • Man with age 18 years or older
  • Couples who could gain fertilized cells after In vitro fertilization (IVF) or Intracytoplasmic sperm injection (ICSI) after hormonal stimulation due to sterility treatments
  • Couples presenting negative blood samples of human immunodeficiency virus (HIV) and Hepatitis B/C
  • Signed routine contracts between hospital and patient wanting assisted reproductive technology (ART)
  • Signed informed study consent
  • Expectation of life more than 18 years
  • No medical contraindication to become pregnant (female)
  • Routine criteria for assisted reproductive techniques

Exclusion criteria (for female):

  • Poor health status acc. to Investigator's judgement
  • Expectation of life below 18 years
  • Risk of ovarian hyperstimulation syndrome
  • Avital cells (cells that do not further develop or die)
  • Treatment due to fertility preservation, e.g. in case of cancer
  • Problems after stimulation and follicle puncture
  • Endometrial pathologies like polyps, submucous fibroids, etc.
  • Any preceding stimulation cycle with endometrial thickness below 6mm
  • Less than 4 fertilized oocytes
  • Patient (and partner) wishes single embryo Transfer
  • Failure to become pregnant with new zygote selection method

Sites / Locations

  • Neue FrauenklinikRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Z-Score and computer algorithm

Z-Score

Arm Description

Outcomes

Primary Outcome Measures

Clinical pregnancy
Clinical pregnancy is defined as a pregnancy diagnosed by ultrasonographic visualization of one or more gestational sacs or definitive clinical signs of pregnancy. It includes ectopic pregnancy.

Secondary Outcome Measures

Ongoing clinical pregnancy
Clinical pregnancy is defined as a pregnancy diagnosed by ultrasonographic visualization of one or more gestational sacs or definitive clinical signs of pregnancy. It includes ectopic pregnancy.
Life Birth
A live birth is defined as the complete expulsion or extraction from its mother of a product of fertilization, irrespective of the duration of the pregnancy, which, after such separation, breathes or shows any other evidence of life, such as heart beat, umbilical cord pulsation, or definite movement of voluntary muscle, irrespective of whether the umbilical cord has been cut or the placenta is attached.

Full Information

First Posted
November 5, 2015
Last Updated
March 20, 2017
Sponsor
Jürgen Weiss
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1. Study Identification

Unique Protocol Identification Number
NCT02610114
Brief Title
Improvement of Cell Selection in Reproductive Techniques
Official Title
A New Method to Improve the Selection of Zygotes in the Context of Assisted Reproductive Medicine. A Randomized Controlled Blinded Monocenter Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2017
Overall Recruitment Status
Unknown status
Study Start Date
December 2015 (undefined)
Primary Completion Date
March 2018 (Anticipated)
Study Completion Date
November 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Jürgen Weiss

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
It is the aim of this trial to use a new computerized cell selection method, in addition to the current and world-wide used scoring system of fertilized oocytes implemented by Scott, to determine whether this leads to an increase in pregnancy rates in women undergoing assisted reproductive techniques.
Detailed Description
It is the aim of this trial to use a new computerized selection method, in addition to the current and world-wide used scoring system of fertilized oocytes (zygotes) implemented by Scott in 1998, to determine whether this leads to an increase in pregnancy rates in women undergoing assisted reproductive techniques. If successful this could in the future lead to a reduction in the numbers of embryos required to achieve a pregnancy. Transferring only one embryo means minimizing the incidence of high order multiple pregnancies. Regularly couples gain several fertilized oocytes (zygotes) due to artificial reproductive techniques. As a routine, these cells are archived using pictures and videos for quality and safety reasons in different stages of development. Because it is planned to transfer only one or two developed embryos to the uterus, investigators have to select the zygotes with the highest potential for implantation and pregnancy. The remaining cells are preserved using vitrification. In the study, investigators use in addition to the established Zygote-score (Z-score) by Scott a new selection method for one group of patients: The quality of the zygotes of all patients is classified according to the described Scott system. Patients are randomized to two groups. Group 1 is the control group without any further intervention. If needed for selection, the quality of the zygotes of the patients of group 2 is additionally scored with a new method. The pictures of the cells, already taken for quality and safety reasons, are taken and the cells surface is analysed using a computer algorithm.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility
Keywords
Assisted reproductive technology (ART), zygotes, Z-score (Zygote Score), Infertility

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
220 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Z-Score and computer algorithm
Arm Type
Experimental
Arm Title
Z-Score
Arm Type
Active Comparator
Intervention Type
Other
Intervention Name(s)
Z-Score and computer algorithm
Intervention Description
In addition to the routine Z-score for zygote selection, if needed, the photographs of the zygotes already taken for quality and safety reasons are analysed using the new computer algorithm. Within a few minutes it generates a score, determining the quality of the cells. The two best cells upon Z-score result and new computer algorithm result are selected for first transfer.
Intervention Type
Other
Intervention Name(s)
Z-Score
Intervention Description
After fertilisation pronuclei and nucleoli can be seen inside the cells by microscope. Routinely, the alignment of nucleoli can be used generating a score, the Z-score 1-4, established by Scott. Two zygotes getting the best Z-score are selected for cell culture and the cells that develop to embryo stage are used for first transfer.
Primary Outcome Measure Information:
Title
Clinical pregnancy
Description
Clinical pregnancy is defined as a pregnancy diagnosed by ultrasonographic visualization of one or more gestational sacs or definitive clinical signs of pregnancy. It includes ectopic pregnancy.
Time Frame
min. 4 weeks after embryo transfer
Secondary Outcome Measure Information:
Title
Ongoing clinical pregnancy
Description
Clinical pregnancy is defined as a pregnancy diagnosed by ultrasonographic visualization of one or more gestational sacs or definitive clinical signs of pregnancy. It includes ectopic pregnancy.
Time Frame
min. 9 weeks after embryo transfer
Title
Life Birth
Description
A live birth is defined as the complete expulsion or extraction from its mother of a product of fertilization, irrespective of the duration of the pregnancy, which, after such separation, breathes or shows any other evidence of life, such as heart beat, umbilical cord pulsation, or definite movement of voluntary muscle, irrespective of whether the umbilical cord has been cut or the placenta is attached.
Time Frame
through study completion, an average of 40 weeks after last menstrual period

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria (for both male and female, couples): Woman with age 18 years or older Man with age 18 years or older Couples who could gain fertilized cells after In vitro fertilization (IVF) or Intracytoplasmic sperm injection (ICSI) after hormonal stimulation due to sterility treatments Couples presenting negative blood samples of human immunodeficiency virus (HIV) and Hepatitis B/C Signed routine contracts between hospital and patient wanting assisted reproductive technology (ART) Signed informed study consent Expectation of life more than 18 years No medical contraindication to become pregnant (female) Routine criteria for assisted reproductive techniques Exclusion criteria (for female): Poor health status acc. to Investigator's judgement Expectation of life below 18 years Risk of ovarian hyperstimulation syndrome Avital cells (cells that do not further develop or die) Treatment due to fertility preservation, e.g. in case of cancer Problems after stimulation and follicle puncture Endometrial pathologies like polyps, submucous fibroids, etc. Any preceding stimulation cycle with endometrial thickness below 6mm Less than 4 fertilized oocytes Patient (and partner) wishes single embryo Transfer Failure to become pregnant with new zygote selection method
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jürgen Weiss, Professor
Phone
+41 41 205 36 06
Email
juergen.weiss@luks.ch
First Name & Middle Initial & Last Name or Official Title & Degree
Roger Getzmann
Phone
+41 41 205 28 40
Email
roger.getzmann@luks.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jürgen Weiss, Professor
Organizational Affiliation
Luzerner Kantonsspital, Neue Frauenklinik
Official's Role
Study Chair
Facility Information:
Facility Name
Neue Frauenklinik
City
Luzern
ZIP/Postal Code
6000 Luzern 16
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jürgen Weiss, Professor
Phone
+41 41 205 36 08
Email
juergen.weiss@luks.ch
First Name & Middle Initial & Last Name & Degree
Roger Getzmann
Phone
+41 41 205 28 40
Email
roger.getzmann@luks.ch
First Name & Middle Initial & Last Name & Degree
Jürgen Weiss, Professor

12. IPD Sharing Statement

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Improvement of Cell Selection in Reproductive Techniques

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