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Effects of Atosiban on clinical outcomes of in vitro fertilization-embryo transfer

Effects of Atosiban on clinical outcomes of in vitro fertilization-embryo transfer

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900022333
Enrollment
Unknown
Registered
2019-04-05
Start date
2019-07-01
Completion date
Unknown
Last updated
2023-10-30

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

Conditions

infertility

Interventions

Experimental group:atosiban
Control group:placebo

Sponsors

Northwest Women's and Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 38 Years

Inclusion criteria

Inclusion criteria: 1. IVF and ICSI women and consent to participate in this study and sign informed consent; 2. Transplantation of fresh or frozen blastocysts failed only once; 3. Single blastocyst transfer (HRT cycle); 4. Endometrial thickness (> 7mm) on HCG day in fresh cycle; 5. Aged between 20 and 38 years old; 6. BMI (< 28) (kg/m2).

Exclusion criteria

Exclusion criteria: 1. severe endocrine disorders (such as hyperthyroidism, hypothyroidism, hyperprolactinemia, etc.) and other systemic diseases (such as hypertension, diabetes, etc.); 2. severe uterine malformations, uterine fibroids and untreated hydrosalpinx were excluded; 3. recurrent miscarrage; 4. severe endometriosis (Ems III or IV); 5. PGS patients; 6. known allergic history of Atoxiban; 7. Participate in other RCT experiments.

Design outcomes

Primary

MeasureTime frame
live birth rate;

Countries

China

Contacts

Public ContactLiu Shan

Northwest Women's and Children's Hospital

123564787@qq.com+86 189 9193 2450

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 8, 2026