The study is conducted at Arash Women's Hospital on all women undergoing the frozen embryo transfer cycle. Patients who signed informed consent will be randomly divided into two groups. The first group will receive GnRH agonist plus hormone replacement therapy for endometrial preparation. Group 2 will receive hormone replacement therapy. The random allocation and final outcome of the study will be assessed by a person who is unaware of the study process. Also, the statistician will be unaware of the study process
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Endometrial thickness
Timeframe: On the day of transfer
Chemical pregnancy
Timeframe: 14 days after transfer
Clinical pregnancy
Timeframe: 12 weeks of pregnancy