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Mild versus conventional ovarian stimulation in expected normal ovarian responders undergoing IVF/ICSI-ET: a multicenter, open-label, parallel-group, randomized controlled trial

Mild versus conventional ovarian stimulation in expected normal ovarian responders undergoing IVF/ICSI-ET: a multicenter, open-label, parallel-group, randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082894
Enrollment
Unknown
Registered
2024-04-10
Start date
2024-08-01
Completion date
Unknown
Last updated
2024-07-15

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

Conditions

Female infertility

Interventions

Mild ovarian stimulation group:Gonadotropins (Gn, including procaine or quinaphrodine) are used at a dose of =125IU/day during the 1st to 5th day of menstruation, and can increase to 150 IU/day accord
Conventional ovarian stimulation group:Each center follows the current antagonist regimen (Gn dose >= 150IU/day), and the current routine luteal support plan (If no special circumstances, recommended

Sponsors

Women's Hospital, School of Medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 38 Years

Inclusion criteria

Inclusion criteria: 1. Female aged = 1.5 ng/mL, and total number of bilateral antral follicle >= 7 at the initiation of cycle. 3. Planning to undergo cycle with single fresh embryo transfer.

Exclusion criteria

Exclusion criteria: 1. Undergoing PGT. 2. Women with contraindications to assisted reproductive technology or uterine diseases that seriously affect implantation. 3. Ovulation disorders. 4. A history of recurrent miscarriage (loss of 2 or more pregnancies). 5. One or both spouses have chromosomal karyotype abnormalities, excluding chromosomal polymorphisms. 6. Untreated hydrosalpinx with imaging evidence before embryo transfer.

Design outcomes

Primary

MeasureTime frame
live birth rate of AGA newborns in the first cycle;

Secondary

MeasureTime frame
E2 level in trigger day ;Cost and quantity used of Gn;OHSS rate;Transferable embryo rate;Biochemical pregnancy rate;Clinical pregnancy rate;Miscarriage rate;Live birth rate;The incidence of pregnancy complications;Birth weight;The incidence of macrosomia;The incidence of low birth weight;Adverse neonatal outcomes and incidence of birth defects;Cycle cancellation rate;

Countries

China

Contacts

Public ContactHuang Hefeng, Zhang Dan

School of Medicine, Zhejiang University Women's Hospital, School of Medicine, Zhejiang University

huanghefg@hotmail.com+86 137 3580 8888

Outcome results

None listed

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