Prostatic Hyperplasia, Benign

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Review clinical trials related to Prostatic Hyperplasia, Benign. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Impact of Long-term Dutasteride Use on Perioperative Outcomes of HoLEP

This study aims to investigate the effects of long-term dutasteride use (a 5-alpha reductase inhibitor) on surgical outcomes in patients undergoing Holmium Laser Enucleation of the Prostate (HoLEP) for benign prostatic hyperplasia (BPH). While some studies suggest that short-term use of these medications can reduce bleeding during surgery, there is limited data on the impact of chronic, long-term use (at least 6 months) specifically during the HoLEP procedure. The researchers will retrospectively analyze patient records to compare two groups: those who used dutasteride for 6 months or longer before surgery, and those who did not use any 5-alpha reductase inhibitors. The primary focus is to determine whether long-term dutasteride treatment leads to a significant difference in surgical bleeding (measured by hemoglobin drop), operation time, and the efficiency of removing prostate tissue (morcellation). The findings will help surgeons better understand how preoperative medication history influences the technical aspects of HoLEP surgery.

Participants needed: 1,000
Trial details
Age: 40-80Biological sex: MaleType: ObservationalSponsor: Ankara City Hospital BilkentUpdated: Apr 6, 2026Locations: 1
Eligibility criteria

Male patients aged 40 to 80 years. [+4]

Patients with a history of previous prostate surgery or pelvic radiotherapy. [+2]

Status: Not yet recruiting

Efficacy/ Safety of Product DNN.65.21.005 in Patients With Benign Prostatic Hyperplasia

To evaluate the safety and efficacy of DNN.65.21.005 versus Combodart® in the treatment of benign prostatic hyperplasia

Participants needed: 218
Trial details
Phase: Phase 3Age: 50+Biological sex: MaleType: InterventionalSponsor: Ache Laboratorios Farmaceuticos S.A.Updated: Dec 8, 2025
Eligibility criteria

Male participants aged 50 years and older. [+2]

History or evidence of prostate cancer. [+7]

Status: Not yet recruiting

Efficacy and Safety of the DTT106 in the Treatment of Erectile Dysfunction Associated With Benign Prostatic Hyperplasia

The purpose of this study is to assess the safety and efficacy of the DTT106 in the treatment of erectile dysfunction associated with benign prostatic hyperplasia

Participants needed: 262
Trial details
Phase: Phase 3Age: 40+Biological sex: MaleType: InterventionalSponsor: EMSUpdated: Feb 20, 2024Locations: 1
Eligibility criteria

men aged 40 years and older. [+4]

Any clinical or physical observation noted during evaluation by the investigatin... [+27]