Benign Prostatic Hyperplasia Clinical Trial
Official title:
Kinetics of the Finasteride Prostate Induced Apoptosis
The aim of this study is to evaluate the mechanisms involved in the apoptosis induced by a treatment of finasteride on benign prostate hyperplasia (BPH). Five sets of patients who need a surgical procedure because of low tract urinary symptoms are randomly attributed to one of five sets of treatment: 0, 7, 14, 21 or 28 days of finasteride treatment before the day of the procedure. Prostate histological fragments are conditioned for molecular and histologic studies.
Status | Active, not recruiting |
Enrollment | 90 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Male |
Age group | 40 Years to 90 Years |
Eligibility |
Inclusion Criteria: - Patients with low tract urinary symptoms needing a surgical procedure - No previous treatment with finasteride - No androgen deficiency; no prostate cancer suspected. |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
France | Centre hospitalier Lyon Sud | Pierre Bénite |
Lead Sponsor | Collaborator |
---|---|
Hospices Civils de Lyon |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Date of the maximum apoptosis in the prostate tissues treated by finasteride | |||
Secondary | Molecular mechanisms involved in BPH finasteride induced apoptosis | |||
Secondary | Decrease in the frequency of the hemorrhagic incidents after the surgical procedure in patients with a treatment using finasteride |
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