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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03833869
Other study ID # 0020-19-WOMC
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 1, 2019
Est. completion date March 2020

Study information

Verified date February 2019
Source Wolfson Medical Center
Contact Hadas Ganer Herman, MD
Phone 9720526206696
Email hadassganer@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The current study aims to assess the effect of assisted hatching on the implantation rate of frozen blastocytes.


Description:

The Zona Pellucida protects the ovum from the penetration of multiple sperm, and from mechanical and physiological damage until the fertilized ovum reaches the uterus. Subsequently, spontaneous hatching occurs, and enables the embryo to attach to the endometrium. The technique of assisted hatching was originally investigated as a means to improve implantation in cases of zona hardening, and is commonly performed in 3-day embryos. In the current study, the investigators aim to investigate the effect of assisted hatching on 5-day frozen embryos.


Recruitment information / eligibility

Status Recruiting
Enrollment 84
Est. completion date March 2020
Est. primary completion date March 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 39 Years
Eligibility Inclusion Criteria:

- In-vitro fertilization patients at the investigators' institution, intended to undergo a transfer of a frozen five-day embryo (blastocyte)

- 18 to 39 years old

- First to third treatment cycle

- Patient has previously had a maximum of four embryos transferred.

Exclusion Criteria:

- Over 40 years old

- Congenital or acquired uterine malformations

- Hydrosalpinx

- Chronic autoimmune diseases

- Embryo intended to be undergo preimplantation genetic diagnosis

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Assisted hatching
Controlled hatching of the zona pellucida in the laboratory prior to embryo transfer

Locations

Country Name City State
Israel Edith Wolfson Medical Center H_olon

Sponsors (1)

Lead Sponsor Collaborator
Wolfson Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Implantation rate Number of gestational sacs demonstrated on ultrasound divided by the number of embryos transferred (expressed as percentage) Five to six weeks following embryo transfer
Secondary Chemical pregnancy Increase and subsequent decrease in beta HCG levels with no evidence of gestational sac on ultrasound Five to six weeks following embryo transfer
Secondary Early spontaneous abortion Spontaneous abortion of pregnancy during the first trimester of pregnancy Up to 15 weeks from embryo transfer
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