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Active clinical trials for "Hyperplasia"

Results 321-330 of 926

Prostate Embolization for Benign Prostatic Hyperplasia

Benign Prostatic Hyperplasia

This is a Phase I/II investigator sponsored FDA-approved Investigational Device Exemption protocol, with the primary goal of determining the safety of prostatic artery embolization (PAE) for benign prostatic hyperplasia. Our primary goal is to document the frequency of side effects, particularly bladder and rectal complications, which may occur as a result of this procedure. Secondarily, the study will provide preliminary data to determine its effectiveness in diminishing obstructive symptoms associated with BPH.

Completed12 enrollment criteria

FLOMAX® Versus HYTRIN® in Patients With the Signs and Symptoms of Benign Prostatic Hyperplasia

Prostatic Hyperplasia

To study the early onset of symptomatic relief afforded by FLOMAX® capsules, 0.4 mg daily as compared to HYTRIN® capsules, 5 mg (with titration) daily in patients with the signs and symptoms of benign prostatic hyperplasia (BPH) To evaluate patient's tolerability to the use of FLOMAX® capsules 0.4 mg daily in comparison to HYTRIN® capsules, 5 mg (with titration) daily for the treatment of the symptoms of benign prostatic hyperplasia

Completed52 enrollment criteria

FLOMAX® Versus Placebo, in Male Patients With Acute Urinary Retention Related to Benign Prostatic...

Prostate Hyperplasia

To establish whether the administration of FLOMAX® improves the outcome of a trial without catheter (TWOC) after an episode of acute urinary retention and to determine whether spontaneous voiding is maintained over the course of six months of active treatment

Completed47 enrollment criteria

Photoselective Vaporization of the Prostate With the GreenLight XPS™ Laser System vs TURP for the...

Benign Prostatic Hyperplasia

The study compares procedural and post procedural outcomes for photoselective vaporization of the prostate (PVP) and transurethral resection of the prostate (TURP) for the treatment of lower urinary tract symptoms due to benign prostatic enlargement causing bladder outlet obstruction. The study requires use of the CE marked GreenLight XPS™ Laser System (GreenLight XPS) or a CE marked monopolar or bipolar loop TURP system for the treatment of benign prostatic hyperplasia (BPH).

Completed33 enrollment criteria

A Study Comparing Mirena and Systemic Progestin for Endometrial Hyperplasia

Endometrial Hyperplasia

Randomized controlled multi-center study with three arms including 200 patients with low risk endometrial hyperplasia. After confirmed diagnosis the patients will receive one of the following treatments: Provera (Medroxyprogesterone (MPA)/progestin) 10 mg per oral treatment for 6 months 10 day each cycle, MPA 10 mg continuously for 6 months, Mirena (Levonorgestrel) impregnated IUD for 6 months.

Completed13 enrollment criteria

Inositol in Preventing Colorectal Cancer in Patients With Colitis-Associated Dysplasia

Colon CarcinomaDysplasia in Crohn Disease2 more

This pilot, randomized phase I/II trial studies how well inositol works in preventing colorectal cancer in patients with abnormal cells (dysplasia) associated with inflammation of the colon (colitis). Patients with colitis-associated dysplasia may have an increased risk of developing colorectal cancer. Inositol is a vitamin-like substance that may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.

Terminated30 enrollment criteria

Efficacy and Safety of S-Equol on Men With Benign Prostatic Hyperplasia

Benign Prostatic Hyperplasia

The purpose of this study is to assess the safety and effectiveness of S-equol in men with benign prostatic hyperplasia.

Completed34 enrollment criteria

Open-Label Extension Study of MCS-2 in the Treatment of Lower Urinary Tract Symptoms (MCS-2-US-c)...

Lower Urinary Tract SymptomsBenign Prostatic Hyperplasia

This is an open-label extension study of another study protocol, MCS-2-US-a. Subjects who have completed the 12-week treatment and procedures under the protocol MCS-2-US-a will be eligible for this study.

Completed4 enrollment criteria

Efficacy of Natural Extract 2007RD01 Combined With Saw Palmetto in Benign Prostatic Hyperplasia...

Benign Prostatic Hyperplasia

The purpose of this study is to determine if the combination of 2007RD01, a natural extract, and saw palmetto lipidic extract, is more effective at treating lower urinary tract symptoms associated with benign prostatic hyperplasia than saw palmetto lipidic extract alone.

Completed6 enrollment criteria

A Study of Silodosin 8 mg Daily for the Treatment of Nocturia in Men With Benign Prostatic Hyperplasia...

NocturiaProstatic Hyperplasia

Silodosin is compared to placebo to determine if it is safe and effective for the treatment of nighttime urination (nocturia) in men with BPH

Completed5 enrollment criteria
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