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The Early Predictive Role of Complement C3 Levels in Embryo Transfer Pregnancy Outcomes and Discussion on Potential Interventions

The Early Predictive Role of Complement C3 Levels in Embryo Transfer Pregnancy Outcomes and Discussion on Potential Interventions

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500109291
Enrollment
Unknown
Registered
2025-09-16
Start date
2025-09-19
Completion date
Unknown
Last updated
2025-09-22

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

Conditions

Reproductive Medicine

Interventions

treatment group (FET):Patientsin the treatment group(FET) received oral aspirin 10 mg twice daily (po BID) combined with subcutaneous enoxaparin sodium 40 mg once daily (SC QD), initiated on the day
control group (FET):Patients in the control group(FET) received no intervention.
treatment group (ET):Patientsin the treatment group (ET) received oral aspirin 10 mg twice daily (po BID) combined with subcutaneous enoxaparin sodium 40 mg once daily (SC QD), initiated on the day o
control group (ET):Patients in the control group (ET) received no intervention.

Sponsors

Hefei Maternity and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 43 Years

Inclusion criteria

Inclusion criteria: (1) Patients aged <= 43 years with cryopreserved embryos, scheduled for frozen embryo transfer (FET), demonstrating good compliance, and having provided informed consent with written signature. (2)Infertile patients aged <= 43 years old who are scheduled to undergo IVF-ET (modified long protocol), diagnosed with tubal factor infertility, with good compliance, and who have provided informed consent and signed the agreement.

Exclusion criteria

Exclusion criteria: Exclusion criteria:Autoimmune disorders (e.g., antiphospholipid syndrome, systemic lupus erythematosus, Sjögren’s syndrome, Hashimoto’s thyroiditis, rheumatoid arthritis, primary or secondary renal diseases, Henoch-Schönlein purpura, undifferentiated connective tissue disease); Endometriosis, uterine fibroids, adenomyosis, or uterine anomalies; Chromosomal abnormalities in either partner; Endocrine disorders; Blood group incompatibility; Active infections or other infectious factors.

Design outcomes

Primary

MeasureTime frame
Live birth rate ;linical pregnancy rate ;Implantation rate;

Secondary

MeasureTime frame
Biochemical pregnancy rate ;Multiple pregnancy rate ;Ectopic pregnancy rate ;Miscarriage rate ;Preterm birth rate ; Fetal growth restriction (FGR) incidence ;Hypertensive disorders of pregnancy incidence ;

Countries

China

Contacts

Public ContactTang Zhixia

Hefei Maternity and Child Health Hospital

tzx1999@163.com+86 159 5516 4659

Outcome results

None listed

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