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Kinetics of the Finasteride Prostate Induced Apoptosis

Civil Hospices of Lyon logo

Civil Hospices of Lyon

Status and phase

Unknown
Phase 4

Conditions

Benign Prostatic Hyperplasia

Treatments

Drug: finasteride

Study type

Interventional

Funder types

Other

Identifiers

NCT00130767
2003.316

Details and patient eligibility

About

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.

Sex

Male

Ages

40 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Patients with low tract urinary symptoms needing a surgical procedure
  • No previous treatment with finasteride
  • No androgen deficiency; no prostate cancer suspected.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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