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Multidimensional evaluation of different dosage forms of goserelin in the treatment of premenopausal HR+ breast cancer patients based on real-world data

Multidimensional evaluation of different dosage forms of goserelin in the treatment of premenopausal HR+ breast cancer patients based on real-world data

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500112684
Enrollment
Unknown
Registered
2025-11-18
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

breast cancer

Interventions

Goserelin implant treatment group:NO
Goserelin microsphere treatment group:NO

Sponsors

First Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Histopathologically confirmed breast cancer; 2. Age >=18 and <=55 years; 3. ECOG score 0~1; 4. Immunohistochemical determination of ER and (or) PR positivity; 5. Serum estradiol (E2) and follicle-stimulating hormone (FSH) levels at premenopausal levels before receiving goserelin treatment; 6. Serum estradiol (E2) and follicle-stimulating hormone (FSH) level testing at 8~28 weeks.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of psychiatric disorders, cognitive dysfunction, and major organic diseases; 2. Patients with concomitant other malignancies; 3. Patients with breast cancer metastasis, recurrence, or death during this period; 4. Patients with concomitant severe infections or severe underlying diseases such as liver, kidney, and cardiovascular and cerebrovascular diseases; 5. Patients with a history of severe allergy or intolerance to the drugs in this study; 6. Patients with severely incomplete medical records affecting the study results;

Design outcomes

Primary

MeasureTime frame
Estradiol 2 (E2);

Countries

China

Contacts

Public ContactGuo Yuanyuan

First Affiliated Hospital of Zhengzhou University

kobe91f@163.com+86 159 3875 6597

Outcome results

None listed

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