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Recruiting NCT05756023

IVF\ICSI Outcome in Women With Polycystic Ovary Syndrome

No phase Interventional PCOS (Polycystic Ovary Syndrome) of Bilateral Ovaries

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: the pregnancy rate at IVF / ICSI cycles.
Who it may be relevant to
Registry conditions: PCOS (Polycystic Ovary Syndrome) of Bilateral Ovaries. Basic parameters: 20 years — 35 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

IVF\ICSI Outcome in Women With Polycystic Ovary Syndrome Compared With Non Polycystic Ovary Syndrome Women

Overview

Polycystic ovarian syndrome (PCOS) occurs in 5% to 10% of all women of reproductive age and 50% of women who present with sub-fertility due to anovulatory infertility . Clear diagnostic criteria for this condition were identified at the consensus meeting of the European Society of Human Reproduction and Embryology and the American Society for Reproductive Medicine .

Detailed description

Sub-fertile women with PCOS will usually benefit from conventional treatments, such as lifestyle changes, ovulation induction, or laparoscopic ovarian drilling, but some will ultimately need assisted reproductive techniques, either if they will need or if they wish, such as controlled ovarian hyperstimulation and IVF.

In these cases, controlled ovarian hyperstimulation is closely related to high drug costs, need for daily injections and frequent monitoring, whereas it sometimes results in an increased rate of cycle cancellations and potential life threatening complications due to ovarian hyperstimulation syndrome and in the retrieval of immature oocytes, leading to poor fertilization and lower cleavage, pregnancy, and live birth rates compared to the conventional IVF cycles ,although this has not been confirmed by other studies .

In addition, ovulation induction is associated with a high risk of multiple pregnancies due to multiple follicular development, so that it has to be individualized and closely monitored.

In-vitro fertilization (IVF) is a common therapeutic modality used in infertile women. IVF has different success rates in different subgroups of patients.

It is necessary to alter the common standard protocols to overcome the potential obstacles in some populations of patients and achieve the best results . Obesity with PCOS status of patient may decrease the fertilization rate and clinical pregnancy chance after IVF (probably by decreasing the oocyte count and increasing the gonadotropin resistance); however, the results of different studies are conflicting

Interventions

  • Procedure the pregnancy rate at IVF / ICSI cycles
    To study and compare other parameters between the PCOS and non PCOS group, and inside the PCOS group itself eg ; patients with PCOS who have ovarian drilling and non drilling PCOS

Primary outcome measures

  • pregnancy rate [Time frame: From baseline to 15 days after the embryo transfere day.]

Eligibility criteria

Inclusion criteria

  • Oligo-ovulation or anovulation.
  • Clinical and/or biochemical hyper androgenesim.
  • Polycystic ovaries.

Exclusion criteria

  • Androgen-secreting tumors (ovarian or adrenal).
  • Adult-onset congenital adrenal hyperplasia.
  • Thyroid diseases.
  • Cushing's syndrome.
  • Diabetes Mellitus.
  • recurrent ICSI failure
  • endocrine, hematologic and autoimmune disorders
  • Non chromosomal and genetic abnormalities
  • Major uterine anomalies, bad surgical history, sever endometriosis, , hydrosalpinx, uterine fibroids
  • Azospermia

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Diagnostic

Study locations

Egypt · 1 center
  • Assuit University hospitals — Asyut

Identifiers

NCT: NCT05756023 · Islam Mahfouz

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗