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Search / Trial NCT01841528

Live Birth After Fresh Embryo Transfer Vs Frozen-thawed Embryo Transfer in Women With Polycystic Ovary Syndrome

Launched by ZI-JIANG CHEN · Apr 23, 2013

Trial Information

Current as of August 02, 2025

Unknown status

Keywords

Polycystic Ovary Syndrome Infertility In Vitro Fertilization Fresh Embryo Transfer Frozen Thawed Embryo Transfer

ClinConnect Summary

This will be a multi-center, prospective, randomized (1:1 ratio)clinical trial of frozen-thawed embryo transfer vs. fresh embryo transfer after a uniform gonadotropin-releasing hormone (GnRH) antagonist protocol in infertile PCOS patients receiving IVF therapy. Qualified 1180 patients are randomized into either of two groups: group A will undergo fresh embryo transfer (590 cases), Group B will undergo elective cryopreservation of all embryos followed by transfer of thawed embryos to a programmed endometrium (590 cases). All of the participants will receive recombinant follicule stimulating ...

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Women diagnosed as PCOS according to Chinese PCOS diagnosis criteria;
  • Women who have ≥1 years history of infertility;
  • Women aged ≥20 and \<35 years old;
  • Women with body weight ≥40kg;
  • * Women who have at least one of the following indications for IVF or ICSI:
  • 1. Ovulation dysfunction and failed to become pregnant from ovulation induction treatment;
  • 2. Tubal factors: unilateral or bilateral tubal obstruction, adhesion, unilateral or bilateral Salpingectomy or tubal ligation;
  • 3. Male factors: oligoasthenozoospermia, obstructive azoospermia;
  • Women who are undergoing their first cycle of IVF or ICSI;
  • Women who retrieved oocytes number \> 3;
  • Women who are capable of giving informed consent.
  • Exclusion Criteria:
  • Women who underwent unilateral ovariectomy;
  • Women diagnosed as uterus abnormality: malformed uterus (uterus unicorns, septate uterus, duplex uterus, uterus bicomis), adenomyosis, submucous myoma, intrauterine adhesion;
  • Women or their partner with abnormal chromosome karyotype including chromosome polymorphism;
  • Women who have experienced recurrent spontaneous abortion (including biochemical pregnancy abortion) more than 2 times;
  • Women with medical condition that represent contraindication to assisted reproductive technology and/or pregnancy;
  • Women who has developed severe OHSS before oocyte pick-up day;
  • Women with retrieved oocytes number ≤3;
  • Women who are unable to comply with the study procedures.

About Zi Jiang Chen

Zi-Jiang Chen is a dedicated clinical trial sponsor focused on advancing medical research and innovation. With a commitment to improving patient outcomes, the organization specializes in the design, management, and execution of clinical trials across various therapeutic areas. Leveraging a robust network of clinical investigators and research institutions, Zi-Jiang Chen strives to adhere to the highest ethical standards and regulatory compliance, ensuring that all trials are conducted efficiently and effectively. Through collaboration and a patient-centric approach, the organization aims to contribute significantly to the development of new therapies and enhance the overall landscape of healthcare.

Locations

Nanjing, Jiangsu, China

Wuhan, Hubei, China

Lanzhou, , China

Hangzhou, Zhejiang, China

Hefei, Anhui, China

Nanjing, , China

Guangzhou, Guangdong, China

Guangzhou, Guangdong, China

Hefei, , China

Lanzhou, Gansu, China

Nanning, Guangxi, China

Nanchang, Jiangxi, China

Shenyang, Liaoning, China

Jinan, Shandong, China

Yantai, Shandong, China

Shanghai, Shanghai, China

Xi'an, Shanxi, China

Patients applied

0 patients applied

Trial Officials

Zi-jiang Chen, MD

Principal Investigator

Repreductive medical hospital affiliated to Shandong University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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