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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05167838
Other study ID # Cairo University obgyn
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 1, 2022
Est. completion date July 1, 2022

Study information

Verified date April 2022
Source Cairo University
Contact Marwa Mo Eid, Ass.prof
Phone 01001225079
Email marwameid2014@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of our study is to compare in vitro fertilization (IVF) outcomes between fresh embryo transfer (ET) and frozen-thawed ET in women with polycystic ovary syndrome (PCOS).


Description:

Eligible women will be randomized to two groups in a ratio of 1:1 . Both the patients and the clinicians will be aware of the allocated arm. The patients (110) will be equally randomized into two groups: Group A will undergo a day 3 fresh embryo transfer after ovarian stimulation, luteal phase support will be started just after follicular aspiration. Group B will have all of their embryo cryopreserved after ovarian stimulation with no luteal phase support after the aspiration and then undergo a frozen-thawed day 3 embryo transfer. Controlled ovarian stimulation will be done using the gonadotropin releasing hormone (GnRH) antagonist protocol then human chorionic gonadotropin( HCG) 5000 IU trigger for final oocyte maturation.


Recruitment information / eligibility

Status Recruiting
Enrollment 110
Est. completion date July 1, 2022
Est. primary completion date June 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria: - Women diagnosed with PCOS according to modified Rotterdam criteria which includes menstrual abnormalities combined with either hyperandrogenism (hirsutism diagnosed by modified Ferriman-Gallwey score or elevated total testosterone level) or polycystic ovaries. - Women ages =20 and <40years old. - BMI less than 35. - Women who have a history of infertility. - All patients will receive adjuvant drugs for ovulation induction (metformin from preceding cycle, cabergoline 1 tab daily for 8 days and 500 cc colloid solution on day of ovum pick up). Exclusion Criteria: - History of unilateral oophorectomy. - Uterine abnormalities such as a malformed uterus (unicornuate, septate uterus), adenomyosis, submucous myoma or intrauterine adhesion. - Severe male factor for infertility such as azoospermia. - History of repeated ICSI trials failure. - Women who are unable to comply with the study procedures.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
fresh embryo transfer
55 patients undergoing fresh embryo transfer after ovarian stimulation followed by luteal phase support
Frozen embryo transfer
55 patients undergoing frozen embryo transfer after ovarian stimulation followed by cryopreservation of all embryos and transfer in another cycle.

Locations

Country Name City State
Egypt Marwa Eid Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical pregnancy rate Transvaginal Ultrasound to detect gestational sac(GS) 35 days after embryo transfer
Secondary Chemical pregnancy rate Serum ß-human chorionic gonadotropin (HCG) will be measured to determine pregnancy after embryo transfer. 14 days after embryo transfer.
Secondary Early ovarian hyperstimulation syndrome rate(OHSS rate) Abdominal ultrasound ,Hematocrit 3 days after follicular aspiration
Secondary Ectopic pregnancy rate BHCG then doubling after 48 hours ,vaginal ultrasound 14 days for BHCG , vaginal US 3 weeks after transfer
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