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The Influence of Different Embryo Transfer Media on Clinical Outcomes in Patients Undergoing in Vitro Fertilization-Embryo Transfer

The Influence of Different Embryo Transfer Media on Clinical Outcomes in Patients Undergoing in Vitro Fertilization-Embryo Transfer

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111943
Enrollment
Unknown
Registered
2025-11-07
Start date
2025-11-17
Completion date
Unknown
Last updated
2025-11-11

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

Conditions

Infertility

Interventions

Experimental group:the embryos were pretreated in hyaluronic acid-enriched transfer medium for 15–30 minutes, then transferred with it.
Control Group:the embryos were transferred with conventional transfer medium.

Sponsors

Suzhou Municipal Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 42 Years

Inclusion criteria

Inclusion criteria: 1. Patients with frozen-thawed embryo transfer. 2. Female age between 20 and 42. 3. Meet one of the following three conditions: Patients with a history of repeated implantation failure. Or, patients with endometrium less than 7mm on the day of endometrial transformation. Or, transferred with non-good quality blastocysts evaluated with Gardner's score

Exclusion criteria

Exclusion criteria: 1. Women who have uterine abnormalities. 2. Untreated severe hydrosalpinx 3. Undergoing oocyte or sperm donation treatment 4. Preimplantation Genetic Testing 5. Women with contraindications to assisted reproductive technologies and pregnancy, or the presence of diseases with a clear impact on pregnancy

Design outcomes

Primary

MeasureTime frame
Clinical Pregnancy Rate;

Secondary

MeasureTime frame
Biochemical Pregnancy Rate;implantation rate;abortion rate;Live birth rate;premature rate;Birth weight;Congenital anomalies;

Countries

China

Contacts

Public ContactJie Ding

Suzhou Municipal Hospital

dj95028@163.com+86 130 5747 6521

Outcome results

None listed

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