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Comparison of the effect of combination of alprosterone and dydrogesterone on luteal support after fresh cycle transplantation

Comparison of the effect of combination of alprosterone and dydrogesterone on luteal support after fresh cycle transplantation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105270
Enrollment
Unknown
Registered
2025-07-01
Start date
2025-07-01
Completion date
Unknown
Last updated
2025-07-07

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

Conditions

Infertility

Interventions

Control group:Dgestprogesterone combined with progestin vaginal sustained-release gel
Experimental group:Aloestrol tablets combined with progesterone vaginal sustained-release gel

Sponsors

The Second Affiliated Hospital Of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 42 Years

Inclusion criteria

Inclusion criteria: 1.Women aged 18 to 42; 2.Use the agonist long regimen to promote ovulation; 3.Planning or transplantation of one or two embryos / blastocysts on fresh IVF cycles D3 or D5; 4.Hormonal tests (FSH, E2, LH, PRL, T, TSH) were normal; 5.BMI range ranges from 18 to 30 kg/m2; 6.Volunteer participate in the study and signed the informed consent;

Exclusion criteria

Exclusion criteria: 1. Known hypersensitivity to the main ingredients or excipients of allyl estradiol tablets (Dolim), dydrogesterone tablets (Daftung) or progesterone soft capsules (Angeltan); 2. Presence of any contraindication to allylsbestradiol tablets (Dolim), dydrogesterone tablets (Daftung) or progesterone soft capsules (Angeltan); 3. Unsuccessful ART embryo transfer (fresh or frozen transfer IVF cycle) > = 3 times; 4. Have a history of recurrent miscarriage (spontaneous abortion >=2 times); 5. Use of any progestogen preparation within 30 days before the egg retrieval date; 6. Acute genitourinary diseases; 7. Contraindications to pregnancy; 8. History of radiotherapy and chemotherapy; 9. Presence of any disease that may affect study completion; 10. Current or recent history of drug abuse, including alcohol and tobacco; 11. Have a history of mental disorder; 12. Participated in any other clinical trial 3 months prior to enrollment; 13. Other conditions judged by the investigator to be unsuitable for participating in this clinical study; 14. Malformations of uterine development;

Design outcomes

Primary

MeasureTime frame
Continuous pregnancy rate;

Secondary

MeasureTime frame
Clinical pregnancy rate;Prevalence of adverse reactions;Rate of abortion;Biochemical pregnancy rate;Multifetal pregnancy rate;Healthy newborn rate;live birth rate;Incidence of adverse events (including neonatal malformations);Preterm birth rate;

Countries

China

Contacts

Public ContactSong Yuxia

The Second Affiliated Hospital Of Zhengzhou University

hnzzsyx@126.com+86 15238633088

Outcome results

None listed

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