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Canceled by the investigator. Effects of ovulation triggered by different trigger regimens on oocyte maturation and assisted pregnancy outcome in normal response to antagonist regimens in assisted reproduction

Effects of ovulation triggered by different trigger regimens on oocyte maturation and assisted pregnancy outcome in normal response to antagonist regimens in assisted reproduction

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400079817
Enrollment
Unknown
Registered
2024-01-12
Start date
2024-01-16
Completion date
Unknown
Last updated
2024-06-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients with normal ovarian response to assisted reproduction

Interventions

hCG group:10000 IUHCG triggers ovulation
GnRH-a group:0.2 mg triptorelin triggers ovulation
Dual trigger group:0.2 mg triptorelin plus1500 IUHCG

Sponsors

Sichuan Academy of Medical Sciences& Sichuan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: women aged 20–35 years with a body mass index (BMI) of 18.5–28 kg/m², anti-Müllerian hormone (AMH) levels of 1.1–4.0 ng/mL, baseline follicle-stimulating hormone (FSH) levels of 3–15 IU/L, and baseline LH levels >3 IU/L. Eligible participants included those with female factor infertility (tubal factors, pelvic adhesions, or mild endometriosis), mild male factor infertility, or unexplained infertility. A normal response was defined as retrieving 4–15 oocytes, with a maximum E2 level <2500 pg/mL, an antral follicle count of 7–14, and those undergoing their first IVF/ICSI treatment.

Exclusion criteria

Exclusion criteria: secondary infertility; poor or high ovarian stimulation response; severe male factor infertility including oligospermia or azoospermia; endocrine disorders such as diabetes mellitus, hyperprolactinemia, thyroid dysfunction, congenital adrenal hyperplasia, Cushing syndrome, polycystic ovary syndrome; uterine abnormalities (endometrial polyps, submucosal fibroids, or myomas with a diameter of =5 cm, uterine cavity adhesions, and septate uterus); and patients who were not candidates for fresh embryo transfer.

Design outcomes

Primary

MeasureTime frame
MII oocyte rate;The number of 2PN embryos;Number of transferable D3 embryos;Number of good-quality D3 embryo;Number of blastocysts formed;Number of good-quality blastocysts;Clinical pregnancy rate;hCG-positive rate;Biochemical pregnancy rate;Early miscarriage rate;Live birth rate;Number of oocytes;Number of follicles >14 mm;

Secondary

MeasureTime frame
Number of embryos transferred;Endometrial thickness on transfer day;Total gonadotropin dose;Days on gonadotropin;Total antagonist dose;Days on antagonist;Basal hormone level;

Countries

China

Contacts

Public ContactLi Linfeng

Sichuan Academy of Medical Sciences& Sichuan Provincial People's Hospital

15982473326@163.com+86 159 8247 3326

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026