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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03240302
Other study ID # HYMC-0069-17
Secondary ID
Status Not yet recruiting
Phase N/A
First received July 31, 2017
Last updated August 2, 2017
Start date September 2017
Est. completion date September 2020

Study information

Verified date August 2017
Source Hillel Yaffe Medical Center
Contact Medeia Michaeli, PhD
Phone 972-50-6246885
Email medeia.michaeli@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this research is to compare sibling oocytes using two sperm selection methods for choosing the best quality spermatozoa before they are injected into oocytes and the influence of each of these methods on embryo quality and IVF outcome.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 50
Est. completion date September 2020
Est. primary completion date September 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Males aged 18-60

- Females aged 18-35

- Males with mild OTA (oligo terato astheno zoospermia) and at least one failed IVF cycle

- Males with normozoospermia with at least 2 unexplained failed IVF cycles

- Females with normal FSH and normal AMH values

- Females who have retrieved in previous cycles at least 6 oocytes

Exclusion Criteria:

- Couples who have been exposed to heavy smoking, drugs and chronic diseases

- Males who have undergone testicular surgery (TESE) or defined as severe OTA

- Females with egg factor infertility

Study Design


Related Conditions & MeSH terms


Intervention

Device:
ICSI petri dish
Half of the oocytes will be placed into the standard ICSI petri dish and they will be injected with sperm with normal morphology.
PICSI petri dish
Half of the oocytes will be placed into a PICSI petri dish (whose bottom is coated with hyaluronic acid) and the mature spermatozoa with CD44 receptors that are attached to the bottom of the dish will be injected into them.

Locations

Country Name City State
Israel Hillel Yaffe Medical Center Hadera

Sponsors (1)

Lead Sponsor Collaborator
Hillel Yaffe Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Comparison of fertilization rate Injected sibling oocytes are incubated in a time-lapse incubator which enables ongoing observation after fertilization and cleavage of each oocyte. The fertilization rates of the ICSI and PICSI methods will be compared. Three years
Primary Comparison of embryo quality Injected sibling oocytes are incubated in a time-lapse incubator which enables ongoing observation after fertilization and cleavage of each oocyte. The embryo quality of the ICSI and PICSI methods will be compared. Three years
Secondary Implantation rate Injected sibling oocytes are incubated in a time-lapse incubator which enables ongoing observation after fertilization and cleavage of each oocyte. The implantation rates of the ICSI and PICSI methods will be compared. Three years
Secondary Pregnancy rate Injected sibling oocytes are incubated in a time-lapse incubator which enables ongoing observation after fertilization and cleavage of each oocyte. The pregnancy rates of the ICSI and PICSI methods will be compared. Three years
Secondary Miscarriage rate Injected sibling oocytes are incubated in a time-lapse incubator which enables ongoing observation after fertilization and cleavage of each oocyte. The miscarriage rates of the ICSI and PICSI methods will be compared. Three years
Secondary Live birth rate Injected sibling oocytes are incubated in a time-lapse incubator which enables ongoing observation after fertilization and cleavage of each oocyte. The live birth rates of the ICSI and PICSI methods will be compared. Three years
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