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Male clinical trials

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NCT ID: NCT04238650 Completed - Healthy Volunteers Clinical Trials

A Pharmacokinetic Study Comparing MB02 And EU Avastin® In Healthy Male Volunteers

Start date: August 2, 2019
Phase: Phase 1
Study type: Interventional

A Randomised, Double Blind, Two-Arm, Single Dose, Parallel Phase I Study To Compare the Pharmacokinetics, Safety and Immunogenicity of MB02 (a Proposed Bevacizumab Biosimilar Drug) and EU Approved Avastin® in Japanese Healthy Male Volunteers. During the course of the study, the similarity in pharmacokinetics will be assessed by sampling the levels of drug in the blood, and by comparing these levels among the different administration arms. Safety, tolerability, and immunologic response to the administered drugs will also be evaluated throughout.

NCT ID: NCT04143399 Completed - Male Clinical Trials

HoLEP vs BPRP of a Large Volume BPH: a Randomised Controlled Trial

Start date: February 14, 2016
Phase: N/A
Study type: Interventional

To compare bipolar resection versus holmium laser enucleation for management of large BPH.

NCT ID: NCT03998150 Completed - Male Clinical Trials

Holmium Laser vs Bipolar Enucleation of a Large Volume BPH: a Randomised Controlled Study

BPH
Start date: November 1, 2016
Phase: N/A
Study type: Interventional

To compare bipolar plasmakinetic enucleation versus holmium laser enucleation for management of large BPH.

NCT ID: NCT03659175 Enrolling by invitation - Elderly Clinical Trials

Characteristic of Intestinal Flora in Male Elderly With Small Intestinal Bacterial Overgrowth

IFOSIBO
Start date: October 15, 2018
Phase:
Study type: Observational

We will focus on the intestinal flora structure, risk factors and clinical features of male elderly with SIBO in our study.

NCT ID: NCT03385161 Completed - Ultrasonography Clinical Trials

Intraprostatic Injection of Botulinum Toxin A Versus Ethanol for Treatment of Patients With Benign Prostatic Hyperplasia

Start date: December 2013
Phase: N/A
Study type: Interventional

To compare safely and efficacy of intraprostatic injection of botulinum toxin A versus ethanol for treatment of benign prostatic hyperplasia (BPH).

NCT ID: NCT02825225 Completed - Prostate Cancer Clinical Trials

A Prospective Randomized Trial of Two Different Prostate Biopsy Schemes

Start date: May 2012
Phase: N/A
Study type: Interventional

The main purpose is to compare the detection rate of 20-core versus 12-core prostate biopsy. The secondary objective is to evaluate pain perception using a validated scale to compare the analgesia provided by the two different local anesthesia schemes. Data will be prospectively collected from patients who will undergo prostate biopsy in a single high volume urology center. The patients will be randomized to two different biopsy samplings and two local anesthesia schemes.

NCT ID: NCT01727960 Recruiting - Adolescents Clinical Trials

The Effect of Education on Decreasing the Prevalence and Severity of Neck and Shoulder Pain

Start date: January 2012
Phase: N/A
Study type: Observational

Neck and shoulder pain (NSP) is fairly common among high school students in Korea. Presumably, the high prevalence of NSP in Korean adolescents is a consequence of an inappropriate static position for a prolonged period of time. We suspect that proper education and posture correction for Korean adolescents may decrease the prevalence or severity of NSP. Although several studies have focused on the etiology of NSP during adolescence, few studies have addressed the management or prevention of NSP in adolescents, despite its high prevalence in this age group. The aims of this prospective study was to identify the effects of education, in terms of recognition of this issue and posture correction, on prevalence and severity of NSP in Korean adolescents

NCT ID: NCT01220388 Completed - Healthy Volunteers Clinical Trials

Effects of L-lysine on Adrenal Secretion

L-Lysine
Start date: October 2010
Phase: N/A
Study type: Interventional

Data from the literature and previous in vitro research conducted in the investigators' laboratory (INSERM U413/EA4310, University of Rouen) suggest that adrenal corticosteroid secretion might be controlled by a paracrine mechanism involving serotonin type IV receptor (5-HT 4). L-lysine, a common amino-acid has been shown to act as a 5-HT4 agonist in vitro as well as in vivo. In the present physiology trial, plasma aldosterone and cortisol levels will be measured under treatment with aprepitant versus placebo, in both basal conditions and after activation of the adrenocortical function by various stimuli, including upright posture, metoclopramide, and after a 3 days salt-free diet. All healthy volunteers will be given two substances (L-lysine and placebo) in a random order during two 13 days periods separated by a 14 day-wash-out. This study should allow to determine the role of 5-HT4 receptors in the control of corticosteroid production in normal man.

NCT ID: NCT01207089 Completed - Healthy Clinical Trials

To Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Oral Administration of AZD8329

AZ8329
Start date: September 2010
Phase: Phase 1
Study type: Interventional

The purpose of the study is to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of AZD8329 following multiple ascending dose administrations in in overweight to obese but otherwise healthy male subjects.

NCT ID: NCT01042249 Completed - Stroke Clinical Trials

Pelvic Floor Muscle Training(PFMT) on Lower Urinary Tract Symptoms (LUTS) in Men With Stroke

Start date: February 2010
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the effect of pelvic floor muscle training (PFMT) on Lower Urinary Tract Symptoms (LUTS) in men after stroke. 120 men with LUTS or increased LUTS after stroke is included and randomized into a treatment group or a control group. The subjects in the treatment group follows a 12 week standard PFMT program, while the control group is not given specific treatment of their LUTS but like the treatment group follows the standard rehabilitation program for stroke patient. Outcome are measured by - 5 questionnaires - Voiding diary - 24-hour pad test - pelvic floor muscle assessment test