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Real-world study for pegfilgrastim(Jinyouli) in preventing neutropenia after chemotherapy in patients with ovarian cancer

Real-world study for pegfilgrastim(Jinyouli) in preventing neutropenia after chemotherapy in patients with ovarian cancer

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900027961
Enrollment
Unknown
Registered
2019-12-07
Start date
2019-12-05
Completion date
Unknown
Last updated
2019-12-10

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

Conditions

ovarian cancer

Interventions

PEG-rhG-CSF group:After 24 hours of chemotherapy, and 12 days before the next cycle of chemotherapy, subcutaneous injection of Jinyouli (PEG-rhG-CSF) 6mg

Sponsors

The Fourth Hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years old; 2. Breast cancer patients diagnosed by pathology or histology; 3. Patients who plan to receive receive chemotherapy, and use jinyuli prophylactically after chemotherapy; 4. Patients with good mental awareness, understand the clinical Investigate and voluntarily join the study and sign an informed consent; 5. Researchers believe that patients can benefit.

Exclusion criteria

Exclusion criteria: 1. Those who have been confirmed to be allergic to pegfilgrastim or rhG-CSF and/or its excipients; 2. Pregnant or lactating women and women who plan to become pregnant during clinical observation; 3. Other patients considered unsuitable by doctors.

Design outcomes

Primary

MeasureTime frame
incidence rate of FN;

Secondary

MeasureTime frame
Incidence of grade IV neutropenia;Incidence and duration of chemotherapy delay (for any reason, chemotherapy delay time is greater than or equal to 3 days);Incidence of chemotherapy dose reduction;Relative dose intensity;

Countries

China

Contacts

Public ContactShan Kang

The Fourth Hospital of Hebei Medical University

ksjq62@sina.com+86 13832325100

Outcome results

None listed

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