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Active clinical trials for "Prostatic Hyperplasia"

Results 471-480 of 588

A Study to Determine the Improvement of the Symptoms of Benign Prostatic Hyperplasia (BPH) When...

Benign Prostatic Hyperplasia

Hypothesis: Dutasteride will perform better than finasteride in decreasing prostate volume, improving symptoms based on International Prostate Symptom score,and lower pvr based on the scientific information that dutasteride inhibits both Type I and II 5-alpha-reducatase vs. finasteride which only inhibits the Type II enzyme

Unknown status7 enrollment criteria

Kinetics of the Finasteride Prostate Induced Apoptosis

Benign Prostatic Hyperplasia

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.

Unknown status3 enrollment criteria

A 20-Week Study of a New Treatment for Men With Benign Prostatic Hyperplasia (BPH).

Prostatic Hyperplasia

Patients who are currently symptomatic and have been diagnosed with BPH by a physician may qualify for this 20-week study. Patients must not be diabetic, must not have prostate cancer and must not have had any surgery to repair your prostate or treat your BPH. Patients will first undergo a phone screening to confirm their eligibility and interest and to rule out any exclusionary history or medications. Eligible patients will be scheduled to come in to the clinic to sign an Informed Consent Form. Patients will then undergo blood and urine tests, a complete physical examination and history and answer several questionnaires to determine their eligibility. Patients will have a total of at least 7-8 visits over 20 weeks to the clinic during this study.Qualified patients receive free study medication, free medical care (physical examinations, EKG, laboratory tests) for the duration of the study.

Unknown status4 enrollment criteria

CLEAR Study: Evaluation of the Safety and Efficacy of the ClearRing System for the Treatment of...

Benign Prostatic HyperplasiaLower Urinary Tract Symptoms

The ProArc Medical ClearRing system is a prostatic reshaping device that is designed to treat Lower Urinary Tract Symptoms (LUTS) due to BPH. During the procedure an implant is delivered into the prostate tissue obstructing the urethra and restricting urine flow. The delivery system uses an electrocutting blade to perform a circular incision, in which the implant is placed. The implant expands the obstructed area, and allows fluid flow through the prostatic urethra

Unknown status11 enrollment criteria

Clinical Study to Assess the Influence of a Saw Palmetto Preparation in Patients With Benign Prostatic...

Sexual Dysfunctions in Men With Benign Prostatic Hyperplasia

Assessment in an open trial if a standardized saw palmetto preparation has a positive influence on sexual dysfunctions in patients with BPH and sexual dysfunctions.

Unknown status9 enrollment criteria

Prostatic Urethral Lift (PUL) Pre-/Post-Radiation Treatment for Prostate Cancer

Benign Prostatic Hyperplasia (BPH)Prostate Cancer

The purpose of this study is to test the use of the Prostatic Urethral Lift (PUL), Urolift®, in prostate cancer (Pca) participants seeking or undergoing radiotherapy for relief of urinary obstructive symptoms.

Withdrawn9 enrollment criteria

The Role of the Seven Sweeps in the Prevention of the Prostate Cancer Among Those With a Positive...

Prostate CancerProstatic Neoplasms1 more

The seven sweeps is a recommended act performed by men after urinating in order to be confident that no urine is left in the urethra, and its not compulsory to perform. It is performed by the following way: after urinating, the anus is first purified if it has become impure; then, the middle finger of the left hand is slid three times from the anus up to the scrotum; then, the thumb is placed on the penis and the forefinger is placed under the penis, and the thumb and forefinger are pulled three times along the penis up to the point of circumcision; finally, the end of the penis is pressed three times.

Completed2 enrollment criteria

Anticoagulant/Antiaggregant Use and Postoperative Bleeding Risk in Patients With Bladder Tumor and...

HematuriaRetention3 more

Patients who were using anticoagulant or antiaggregant medications for any reason and underwent transurethral resection of bladder tumor (TUR-BT) or transurethral resection of the prostate (TURP) or open prostatectomy (OP) due to BPH will be compared with those who were not using anticoagulant or antiplatelet medication. The rates of postoperative clot retention, presence of hematuria, reoperation due to hematuria, blood transfusion and re-admissions due to hematuria in the first postoperative month will be compared.

Completed6 enrollment criteria

An Observational Study of Radial Access Embolization Procedures Using HydroPearl Microspheres

Uterine FibroidArteriovenous Malformations2 more

This registry study is designed to collect data on the procedural success and complication rates in real-world patients undergoing HydroPearl embolization procedures via radial access.

Completed7 enrollment criteria

Embozene® Microspheres for Prostatic Arterial Embolization in Patients With Symptomatic Benign Prostatic...

Benign Prostatic Hyperplasia

The purpose of this observational study is to evaluate the prostatic arterial embolization (PAE) with Embozene® Microspheres (Boston Scientific) in sphere sizes of 250 µm for the treatment of symptomatic benign prostatic hyperplasia (BPH).

Completed18 enrollment criteria
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