Prolonged Protocol of Early Follicular or Mid Luteal Phase

  • STATUS
    Recruiting
  • End date
    May 13, 2024
  • participants needed
    1150
  • sponsor
    Second Affiliated Hospital of Wenzhou Medical University
Updated on 24 January 2021
gonadotropin
infertility
antral
polycystic ovary syndrome
embryo transfer
controlled ovarian hyperstimulation
antral follicle count
ovarian hyperstimulation

Summary

Due to the injection of gonadotropin releasing hormone agonist (GnRH-a) before controlled ovarian hyperstimulation (COH), the scheme of prolonged early follicular period protocol has obvious advantages in achieving ideal egg number, increasing endometrial receptivity to embryo transfer, inhibiting endogenous luteinizing hormone (LH) peak and reducing cycle cancellation rate. The full dose of long acting GnRH-a was also applied before COH in the mid luteal Hypergrowth program, and the mechanism of its lowering tone was similar. But whether the clinical and perinatal outcome of early follicular hyperlengthening is as effective as that of mid luteal hyperlengthening has not been reported at home and abroad. Moreover, there is a lack of prospective randomized controlled studies.

Description

One injection of 3.75mg GnRHa was injected on the 1st-3rd or 21st-23rd day of menstruation. The level of estradiol (E2), progesterone (P), luteinizing hormone (LH) in peripheral blood and the number of follicles in bilateral ovarian internal sinuses were monitored on the 32nd-38th day after pituitary hyporegulation.Gonadotropin (Gn) will be given after pituitary desensitization. When the diameter of at least two follicles 18mm or more than three follicles 17mm, the trigger of human chorionic gonadotropin (hCG) will be given and oocyte will be retrieved. The selective fresh single blastocyst transplantation will be carried out on the 4th-6th day after oocyte retrieval. HCG test at 12nd day after transplatation. Follow-up investigation will given during the pregnancy and perinatal period.

Details
Condition assisted reproductive technology, In Vitro Fertilization, In Vitro Fertilization, assisted reproductive technologies
Treatment Change the injection time of long acting GnRH-a
Clinical Study IdentifierNCT04522479
SponsorSecond Affiliated Hospital of Wenzhou Medical University
Last Modified on24 January 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Tubal factor infertility
polycystic ovary (PCO) or polycystic ovary syndrome (PCOS) patients
Patients of mild to moderate endometriosis
Oligoasthenospermia in male
More than 5 antral follicle count (AFC) on both ovaries
Unexplained infertility: there is a history of no contraception and pregnancy for more than 1 year, no clear cause of infertility such as ovulation, fallopian tube, endometrium and male factors is found, or the above factors return to normal after treatment

Exclusion Criteria

History of adverse pregnancy and childbirth
Unilateral ovariectomy
Uterine malformation, intrauterine adhesion, submucous myoma
Chromosomal abnormality of both husband and wife
Patients with contraindications of assisted reproductive technology or pregnancy: such as uncontrolled diabetes mellitus, undiagnosed liver and kidney dysfunction, history of deep vein thrombosis, history of pulmonary embolism, history of cerebrovascular accident, uncontrolled hypertension, heart disease, suspected cervical cancer, endometrial cancer, breast cancer or previous history, undetermined vaginal bleeding
Unable to be regularly follow up
Participating in other clinical trials
No fresh single blastocyst transfer
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