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A randomized crossover trial on the preference of different preparations of goserelin for androgen deprivation therapy (ADT) in patients with prostate cancer

A randomized crossover trial on the preference of different preparations of goserelin for androgen deprivation therapy (ADT) in patients with prostate cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111711
Enrollment
Unknown
Registered
2025-11-04
Start date
2024-06-18
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

Prostate cancer

Interventions

Experiment 1:The patient was first injected with two cycles of Norrade and then received two cycles of Bactovir
Experiment 2:First, inject two cycles of Biotovir and then receive two cycles of Norrade

Sponsors

The First Affiliated Hospital of Xiamen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Prostate cancer confirmed by histology; 2. Age >=18 years old; 3.ECOG score: 0-2 points; 4. The researcher determined that ADT drug treatment was necessary; 5. Has not received ADT drug treatment in the past or has been using ADT for less than 6 months and has stopped for more than 6 months; 6. Life expectancy > 1 year; 7. Good liver and kidney functions; 8. Good compliance;

Exclusion criteria

Exclusion criteria: 1.;Diagnosed or suspected hormone resistant prostate cancer with pituitary resection, adrenalectomy or pituitary lesions; 2.History of cardiovascular events, uncontrolled hypertension, gastrointestinal diseases that interfere with treatment absorption, active viral hepatitis or active human immunodeficiency infection in the past 6 months; 3.There is any disease that the investigator believes makes the patient unfit to participate in the study;

Design outcomes

Primary

MeasureTime frame
Patient preference for medication choice;

Secondary

MeasureTime frame
Pain at injection site;Incidence of local adverse reactions at the injection site of ADT;Quality of life of patients during treatment;Serum testosterone;The PSA level during ADT treatment;Fatigue of patients during treatment;

Countries

China

Contacts

Public ContactXuegang Wang

The First Affiliated Hospital of Xiamen University

stefwxg@163.com+86 592 213 9714

Outcome results

None listed

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