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Clinical Study on the Safety and Efficacy of Tuopei Filgrastim Injection in Patients with Reproductive Disorders

Clinical Study on the Safety and Efficacy of Tuopei Filgrastim Injection in Patients with Reproductive Disorders

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500101241
Enrollment
Unknown
Registered
2025-04-22
Start date
2025-05-08
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Reproductive disorders

Interventions

Petinotherapy group:NA
G-CSF/ petinotherapy group (short-acting G-CSF followed by petinotherapy),:NA
Short-acting G-CSF group:NA
control group (patients receiving only basal medication and/or other prophylactic or therapeutic regiments, but not receiving any G-CSF):NA

Sponsors

The Second Hospital of Lanzhou University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1.Patients aged between 18 and 45 years (inclusive of 18 and 45 years); 2.Patients with recurrent miscarriage and/or previous implantation failure; 3.The administration route for Tuopei Filgrastim Injection and other G-CSF agents is subcutaneous injection.

Exclusion criteria

Exclusion criteria: 1. Severe hepatic, renal, cardiac, or pulmonary dysfunction; 2. Pregnant women with a history of severe diseases or severe mental disorders.

Design outcomes

Primary

MeasureTime frame
Adverse events ;

Secondary

MeasureTime frame
Continuous clinical pregnancy rate at 12 weeks gestation;Continuous clinical pregnancy rate at 24 weeks gestation;Spontaneous early abortion rate;

Countries

China

Contacts

Public ContactFang Wang

The Second Hospital of Lanzhou University

ery_fwang@lzu.edu.cn+86 139 1930 2888

Outcome results

None listed

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