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Hypertrophy clinical trials

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NCT ID: NCT00466544 Not yet recruiting - Tonsillitis Clinical Trials

Randomized Controlled Study of Plasmaknife Tonsillectomy Versus Monopolar Tonsillectomy

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Start date: May 2007
Phase: Phase 4
Study type: Interventional

Study objective is to provide prospective randomized controlled data on pediatric pain levels found in PlasmaKnife tonsillectomy and monopolar tonsillectomy.

NCT ID: NCT00461123 Completed - Clinical trials for Prostatic Hypertrophy, Benign

Vardenafil in Greenlight(TM) Laser Surgery of Benign Prostate Hypertrophy

Start date: March 2007
Phase: Phase 2
Study type: Interventional

The greenlight laser has an absorption maximum which is exactly the same as for hemoglobin. In the presence of hemoglobin, its application causes vaporization of the tissue and this effect depends on the concentration of hemoglobin in the respective tissue. Therefore, increase of blood-flow in the tissue (here: prostate gland) should exert better efficacy of the laser application and consequently shortening of the required duration of laser application.

NCT ID: NCT00459927 Withdrawn - Clinical trials for Obstructive Sleep Apnea

Comparison of Floseal Hemostasis Tonsillectomy With Coblation Tonsillectomy and Cautery Hemostasis Tonsillectomy

Start date: July 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to evaluate a new method of hemostasis, floseal gel, in tonsillectomy and adenoidectomy, with the goal of decreasing post operative and intraoperative morbidity.

NCT ID: NCT00449150 Terminated - Clinical trials for Benign Prostatic Hypertrophy

Cetrorelix (CET) Pamoate Regimens in Patients With Symptomatic Benign Prostatic Hypertrophy (BPH)

Start date: March 2007
Phase: Phase 3
Study type: Interventional

Benign Prostatic Hypertrophy (BPH) is a common and bothersome condition of aging men. It is characterized by an enlargement of the prostate occurring in human male over the age of 50 which increases in prevalence with age, and among those aged 50 to 80, about 40% report moderate or severe urinary symptoms of prostatism. The aim of treatment is to improve patients' quality of life which primarily depends on the severity of the symptoms of BPH. Current treatments of BPH have a benefit / risk ratio which leaves room for improvement. For this study, study medication (Cetrorelix pamoate or placebo) is administered by injection in the buttocks (Intramuscular). All patients completing the double-blind portion (Week 0 to 52) are eligible to receive the active drug during the open-label part of the study (Week 52 to 90).

NCT ID: NCT00446563 Completed - Clinical trials for Hypertension; Hypertrophy, Left Ventricular

Efficacy and Safety of Valsartan in Combination With Amlodipine Compared to Losartan Plus Hydrochlorothiazide in Patients With Hypertension and Left Ventricular Hypertrophy

Start date: March 2007
Phase: Phase 3
Study type: Interventional

This study will evaluate the safety and efficacy of amlodipine plus valsartan in patients with hypertension and left ventricular hypertrophy

NCT ID: NCT00430833 Active, not recruiting - Clinical trials for Hypertrophic Cardiomyopathy

CHANCE - Candesartan in Hypertrophic Cardiomyopathy

Start date: n/a
Phase: Phase 2
Study type: Interventional

The primary hypothesis of the study is that treatment with AT1-R antagonist in patients with nonobstructive form of HCM will be first save, second will cause regression of myocardial hypertrophy.

NCT ID: NCT00427219 Completed - Clinical trials for Benign Prostatic Hypertrophy

The Safety and Efficacy of Ozarelix to Treat Men With Lower Urinary Tract Symptoms Due to Enlargement of the Prostate

Start date: January 23, 2007
Phase: Phase 2
Study type: Interventional

This study is to compare the efficacy and safety of ozarelix 15 mg given intramuscular (IM) 2 weeks apart on the improvement of symptoms and the duration of improvement for up to 6 months in men with Benign Prostatic Hypertrophy (BPH) who are over 50 years of age.

NCT ID: NCT00418041 Active, not recruiting - Heart Failure Clinical Trials

Chronic Heart Failure Analysis and Registry in the Tohoku District 2 (CHART-2 Study)

Start date: October 2006
Phase: N/A
Study type: Observational

Chronic Heart Failure Analysis and Registry in the Tohoku District 2 (CHART-2 Study) is a large, prospective, hospital-based cohort study to investigate the following: - Characteristics of patients with chronic heart failure and prognostic risks of these patients. - Characteristics of patients with high risk for heart failure and critical factors which predict the development of symptomatic heart failure in these patients. - The incidence and prognostic impact of metabolic syndrome in patients with chronic heart failure. - The association between metabolic syndrome and the development of symptomatic heart failure.

NCT ID: NCT00382356 Completed - Clinical trials for Benign Prostatic Hypertrophy

Dutasteride After Failure of Finasteride In the Management of Symptomatic Prostatic Enlargement/Hypertrophy (BPE/H)

Start date: November 2004
Phase: N/A
Study type: Interventional

The study is to determine the safety and efficacy of Dutasteride in patients who have failed Finasteride therapy for their symptomatic benign prostatic enlargement/ hypertrophy (BPE/H).

NCT ID: NCT00368147 Completed - Clinical trials for Arteriovenous Fistula

Access Creation for Hemodialysis: Association With Structural Changes of the Heart

Start date: April 2002
Phase:
Study type: Observational

The purpose of this study is to determine if the creation of a fistula or a graft plays a role in the development of heart disease for patients undergoing hemodialysis