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
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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
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
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
Similar Trials