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Active clinical trials for "Hyperplasia"

Results 511-520 of 926

Treatment of Refractory Urinary Retention Secondary to Benign Prostatic Hyperplasia (BPH) With Dual...

Urinary RetentionBenign Prostatic Hyperplasia

To determine whether the addition of a dual Five Alpha Reductase Inhitor (Dutasteride) will alleviate urinary retention secondary to BPH in who have failed a voiding trial without a catheter. Following treatment with an Alpha Blocker alone.

Completed14 enrollment criteria

Study to Treat Patients Who Have Signs and Symptoms of Benign Prostatic Hyperplasia (BPH) With Tadalafil...

Benign Prostatic Hyperplasia

The purpose of this study is to determine whether an experimental drug known as tadalafil given once daily can reduce the symptoms associated with Benign Prostatic Hyperplasia (straining, urinary frequency, feeling like your bladder is still full, etc.)

Completed16 enrollment criteria

Botulinum Toxin Injection for the Management of BPH

Benign Prostatic Hyperplasia

This is a double-blind randomized phase II trial to determine whether two different doses of BoNT/A injection into the prostate gland demonstrate sufficient improvement in the management of lower urinary symptoms due to BPH to warrant more extensive research. Subjects will receive either a 100U or 300U dose. Participation will last 1 year.

Completed33 enrollment criteria

TOCILIZUMAB IN FIBROUS DYSPLASIA OF BONE

Fibrous Dysplasia of Bone

Bone pain due to fibrous dysplasia of bone is usually treated with bisphosphonates. A small proportion of patients fail to respond adequately. Mutated bone cells produce large amounts of Interleukin-6 (IL-6), with increased bone resorption as a result. Inhibition of IL-6 may be of interest to reduce bone resorption and therefore bone pain. TOCIDYS is a placebo-controlled randomized cross-over trial to test the hypothesis that tocilizumab can reduce bone resorption in those patients with fibrous dysplasia who have already received bisphosphonates.

Completed8 enrollment criteria

Evaluating a Pharmacokinetic Drug Interaction Between Tadalafil and Tamsulosin

Erectile DysfunctionBenign Prostatic Hyperplasia

We investigate the potential pharmacokinetic drug-drug interaction between Tadalafil and Tamsulosin in healthy male volunteers who receive Tadalafil alone, Tamsulosin alone, and both together in a 3 period repeatedly.

Completed6 enrollment criteria

Determine the Bioequivalence of Two Formulations of Tamsulosin HCl Capsules in Fasted Male.

Prostatic Hyperplasia

A bio-equivalence of 2 different capsule formulations in fasted subjects

Completed2 enrollment criteria

Urodynamic Feasibility Study Utilizing the UroLift® System

Benign Prostatic Hyperplasia

UDS evaluates the impact of Prostatic Urethral Lift (PUL) as measured by pressure flow, urodynamic testing (UDS) and an optional UroCuff Testing, an alternative urodynamic test. In addition, standard BPH measures such as symptoms, qualify of life, uroflowmetry, and post void residual will be evaluated at screening and at the follow-up visits.

Completed38 enrollment criteria

Prostatic Resection Cavity Stone Post Transurethral Resection of the Prostate (TURP). A Rare Case...

Prostate Hyperplasia

Prostatic resection cavity stone post transurethral resection of the prostate (TURP). A rare case scenario

Completed2 enrollment criteria

Total Intravenous Anaesthesia (TIVA) Versus Spinal Anaesthesia in Patients Undergoing Transurethral...

ProstateHyperplasia

Comparison of total intravenous anaesthesia with spinal anaesthesia in patients undergoing transurethral prostate resection

Completed8 enrollment criteria

Effect of Dutasteride on HIF-1alpha and VEGF in the Prostate

Benign Prostatic Hyperplasia

The purpose of this study is to determine whether dutasteride may influence the expression of angiogenesis factors such as hypoxia inducible factor (HIF)-1alpha and vascular endothelial growth factor (VEGF) in patients with lower urinary tract symptoms/benign prostatic hyperplasia (LUTS/BPH).

Completed14 enrollment criteria
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