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Comparison of delayed start antagonist protocol and conventional antagonist regimens in poor ovarian response women: a single center prospective randomized controlled study

Comparison of delayed start antagonist protocol and conventional antagonist regimens in poor ovarian response women: a single center prospective randomized controlled study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078356
Enrollment
Unknown
Registered
2023-12-06
Start date
2023-12-06
Completion date
Unknown
Last updated
2023-12-10

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

Conditions

Infertility

Interventions

pretreatment group:GnRH antagonist administration from day 2 of the menstrual cycle for 3 days
control group:No GnRH antagonist administration from day 2 of the menstrual cycle for 3 days

Sponsors

Northwest women and children’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
35 Years to 42 Years

Inclusion criteria

Inclusion criteria: (1) IVF patients with antagonist protocol (2) Age: 35-42 years old (3) Uneven follicles during initiation: Maximum follicle diameter on day D2 of menstruation - minimum follicle diameter = 3-4mm

Exclusion criteria

Exclusion criteria: (1) Oocyte donation cycles (2) Body mass index>=28 kg/m2 (3) Uterine anatomical abnormalities, endometrial or myometrial lesions: Uterine malformations (unicorn uterus, bicornuate uterus, bicornuate uterus, mediastinal uterus); Adenomyosis of the uterus; Patients with uterine fibroids (fibroids larger than 3cm or closely related to the endometrium); Submucosal uterine fibroids; Uterine adhesions; Untreated endometrial polyps. (4) There is unilateral or bilateral hydrosalpinx that has not been surgically removed or ligated. (5) Endocrine disorders, such as hyperprolactinemia and thyroid diseases with abnormal TSH (6) Recurrent spontaneous abortion (= 2 clinical abortions) 3 IVF attempts, or multiple implantation failures (no clinical pregnancy after surgery) = 3 transplants, with less than one high-quality embryo transferred each time (7) According to the revised American Society of Reproductive Medicine classification (1985), stage III-IV endometriosis. (8) Frozen oocytes, pre implantation genetic testing, or chromosomal karyotype abnormalities in spouses (9) The use of combination therapy or any other situation where the researcher believes that interfering with the trial or cannot ensure the safety and effectiveness of the data.

Design outcomes

Primary

MeasureTime frame
cumulative ongoing clinical pregnancy rate (>12 weeks);

Secondary

MeasureTime frame
Number of retrieved oocytes;Oval corona cumulus sinus follicle index;cumulative active yield;

Countries

China

Contacts

Public ContactShi Wenhao

Northwest Women’s and Children’s Hospital

swihao@126.com+86 29 8721 9120

Outcome results

None listed

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