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Healthy live birth rate after natural ovulation regimen versus programmed regimen for endometrial preparation in ovulatory women undergoing frozen embryo transfer: a randomized controlled trial

Healthy live birth rate after natural ovulation regimen versus programmed regimen for endometrial preparation in ovulatory women undergoing frozen embryo transfer: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200057990
Enrollment
Unknown
Registered
2022-03-25
Start date
2022-07-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Infertility

Interventions

Natural cycles group:Natural ovulation regimen for frozen embryo transfer
Programmed cycles group:Programmed regimen for frozen embryo transfer

Sponsors

Center for Reproductive Medicine, Cheeloo College of Medicine, Shandong University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Women with regular menstrual cycles, which are defined as the length of the menstrual cycle ranging from 24 to 38 days. 2. Women aged >= 20 and <= 40 years. 3. Women who are planning to receive a single frozen-thawed blastocyst transfer, which was derived from IVF cycles, ICSI cycles, or PGT-A cycles. 4. Women with at least one vitrified blastocyst in storage for IVF or ICSI cycles, or one euploid blastocyst for PGT-A cycles; the blastocyst was morphologically graded as 4BC or better using Gardner grading criteria and was cryopreserved on Day 5 or Day 6 of embryo culture.

Exclusion criteria

Exclusion criteria: 1. Women who failed to achieve clinical pregnancy after two or more previous cycles of embryo transfer. 2. Women whose embryos are derived from oocyte donation, frozen oocyte, or embryos that have undergone thawing and re-cryopreservation process. 3. Women with a history of intrauterine adhesion or with untreated submucosal uterine fibroids. 4. Women with untreated hydrosalpinx that is visible under pelvic ultrasound. 5. Women with a history of cycle cancellation due to thin endometrium (<7mm). 6. Anti-phospholipid antibody syndrome, systemic lupus erythematosus, or rheumatologic disease that requires chronic systemic medications. 7. Women who have contraindications for estrogen and progesterone administration (e.g., breast cancer, or risks of venous thromboembolism).

Design outcomes

Primary

MeasureTime frame
Healthy live birth rate;Incidence of preeclampsia/eclampsia;

Secondary

MeasureTime frame
Cycle cancellation rate;Conception rate;Clinical pregnancy rate;Pregnancy loss rate;Live birth rate;Birth weight;Incidence of neonatal complications;Incidence of other adverse events;Incidence of hypertensive disorders of pregnancy;Incidence of gestational diabetes;Incidence of placenta previa;Incidence of placental abruption;Incidence of placenta accreta spectrum;Incidence of premature rupture of membrane;Incidence of stillbirth;Incidence of postpartum hemorrhage;Incidence of preterm birth;

Countries

China

Contacts

Public ContactZi-Jiang Chen

Center for Reproductive Medicine, Cheeloo College of Medicine, Shandong University

chenzijiang@hotmail.com+86 531 8586 1173

Outcome results

None listed

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