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Edessy ICSI Outcome Embryo Score (EIOS) Efficacy

A

Al-Azhar University

Status and phase

Completed
Phase 2
Phase 1

Conditions

Infertility

Treatments

Other: Edessy ICSI Outcome Embryo Score

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Purpose of this study is to detect outcome of intracytoplasmic sperm injection (ICSI) according to EIOS

Full description

A total of 243 infertile couples underwent long GnRH agonist protocol in the ART unit, International Islamic Center for Population Studies and Research (IICPSR), Al-Azhar University.

Embryos which reached the two cell stage at 25-27 hr were classified as EC, and the remaining as Non Early Cleavage embryos (NEC). Embryos were assessed again at 64-68 hours post-ICSI for day three embryo morphology score (Loi et al.,2008). The best two or three embryos, according to day 3 embryo morphology were transferred. Each patient was given a score according to EIOS (female age, number of retrieved oocytes, number of EC embryos, number of good quality embryos and number of embryos transferred).

Enrollment

243 patients

Sex

Female

Ages

20 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≤ 40 years old. BMI >25 - 30 kg/m2. Have two ovaries. Regular cycles. 1st ICSI cycle. Long midluteal GnRH protocol

Exclusion criteria

uterine factor as a cause of female factor infertility. pelvic masses or diseases (e.g: endometriosis, fibroids, hydro- salpnix, ...). history of medical disorders (e.g: hypertension, D.M, thyroid dysfunction, liver diseases, renal diseases,...).

azoospermia as a cause of male factor infertility.

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

243 participants in 1 patient group

Edessy ICSI Outcome Embryo Score
Experimental group
Description:
ICSI
Treatment:
Other: Edessy ICSI Outcome Embryo Score

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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