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Hypertrophy clinical trials

View clinical trials related to Hypertrophy.

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NCT ID: NCT03415750 Completed - Clinical trials for Hypertrophy, Left Ventricular

Everolimus and Tacrolimus Combination for Regression of Left Ventricular Hypertrophy in Renal Transplants

ENHVIE
Start date: November 2016
Phase: Phase 4
Study type: Interventional

Clinical study with two parallel group to compare the efficacy of everolimus combination + tacrolimus in regression of left ventricular hypertrophy vs tacrolimus + mycophenolate mofetil in renal transplant patients in the maintenance phase.

NCT ID: NCT03403621 Terminated - Hypertrophic Scar Clinical Trials

Hypertrophic Scar Prevention by Novel Topical Gel Application

Start date: March 5, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

Researchers are trying to find out more about the side effects of topical (applied to the skin) Pentamidine, to determine if it is safe for use in people. They also want to find out if topical use of Pentamidine can help treat hypertrophic scars. Pentamidine is a medicine that is currently used to treat certain kinds of infection. It is most often given by intravenous (into a vein) or inhalation (through a breathing device). This medication is approved by the U.S. Food and Drug Administration (FDA) for use in these forms. Everyone in this study will receive topical Pentamidine (TP) in a silicone based gel (PCCA Pracasil Plus). Topical treatment of Pentamidine is still experimental and has not been formally tested for safety or effectiveness in a randomized control trial within the United States. The FDA has allowed the use of topical Pentamidine in this research study.

NCT ID: NCT03376620 Completed - Hypertrophic Scar Clinical Trials

Role of Topical Putrescine (Fibrostat) for Prevention of Hypertrophic Scars in Mammoplasty Patients

Start date: September 2, 2011
Phase: Phase 3
Study type: Interventional

Linked to previous Clinical Trial E92:069 in which biochemical effect of 1,4 diaminobutane was studied in human scar harvested at revision surgery after a 12 week application. Analytical data was collected in this phase of the work completed in 1999. This was then followed by clinical correlation in a scar prevention model with topical application of 1,4 diaminobutane for 12 weeks and measuring duredness , as well photographic and POSAS score data for quality of scar formation.

NCT ID: NCT03376464 Completed - Clinical trials for Masseter Muscle Hypertrophy

Xeomin Cosmetic in the Management of Masseter

Start date: November 6, 2015
Phase: Phase 4
Study type: Interventional

The goal of this study was to evaluate the efficacy and safety of two injection techniques in the management of masseteric hypertrophy using Xeomin Cosmetic.

NCT ID: NCT03369990 Not yet recruiting - Clinical trials for Benign Masseteric Hypertrophy

DWP450 Treatment in Subjects With Benign Masseteric Hypertrophy

Start date: December 2017
Phase: Phase 2
Study type: Interventional

This study is A Randomized, Double-blind, Placebo-controlled, Phase II Optimal Dose-finding Study to Determine the Safety and Efficacy of DWP450 in Subjects with Benign Masseteric Hypertrophy

NCT ID: NCT03366194 Completed - Clinical trials for Cicatrix, Hypertrophic

The Clinical Efficacy And Safety Of SkinStylus Microneedling System

Start date: November 15, 2017
Phase: N/A
Study type: Interventional

The purpose of the trial is to provide objective evidence the SkinStylus may be used safely and effectively for the treatment of ventral torso hypertrophic scars.

NCT ID: NCT03335332 Completed - Clinical trials for Hypertrophic Cardiomyopathy

High Intensity Exercise for Increasing Fitness in Patients With Hypertrophic Cardiomyopathy

Start date: January 31, 2018
Phase: N/A
Study type: Interventional

Although current clinical guidelines stipulate that patients with hypertrophic cardiomyopathy should not partake in high intensity exercise (HIE) or competitive sport due to safety concerns, there is no clear evidence to support this notion. In fact, two exercise training interventions in this population indicates that regular moderate to vigorous intensity exercise is efficacious for improving exercise capacity and cardiorespiratory fitness, and does not increase arrhythmia burden or adverse events. Moreover, moderate intensity exercise and HIE training significantly increases cardiorespiratory fitness in patients with cardiac disease. Such improvements are associated with substantial reductions in cardiovascular mortality and might outweigh the risk of adverse events in patients with hypertrophic cardiomyopathy (HCM). Having a genetic cardiomyopathy does not grant immunity against lifestyle related cardiometabolic diseases and inactivity is rife in HCM patients likely due to misinformation/education. It is therefore paramount to further explore the benefits of regular moderate intensity exercise and HIE in patients with HCM for proper therapeutic management of the condition.

NCT ID: NCT03332745 Completed - Aortic Stenosis Clinical Trials

Mechanism of Decompensation Evaluation - Aortic Stenosis

MODE-AS
Start date: September 3, 2018
Phase:
Study type: Observational

Aortic stenosis is the most common heart valve disease requiring intervention in high income countries. It is characterised by progressive valvular thickening, and restriction as well is hypertrophy and fibrosis of the left ventricle in response to pressure overload. The pathological processes in the left ventricle that ultimately result in heart failure and death are incompletely understood. Further elucidation of these processes and how they correlate with novel blood biomarkers may help us design new treatments and optimise the timing of surgical intervention. In brief, recruited patients with severe aortic stenosis and scheduled to undergo valve replacement surgery will be invited for some simple tests (blood sampling, ECG, echocardiogram). A septal myocardial biopsy will be taken at the time of surgery and the disease valve retained. These will be examined histologically and pathological changes compared with results obtained from ECG, echocardiogram and blood tests.

NCT ID: NCT03327623 Recruiting - Clinical trials for Hypertrophic Cardiomyopathy

Sleep Apnea and Hypertrophic Cardiomyopathy (HCM)

Start date: November 13, 2017
Phase:
Study type: Observational

The investigators are trying to find out how common sleep apnea is in hypertrophic cardiomyopathy. The purpose of this study is to see if sleep apnea is common in hypertrophic cardiomyopathy and if its presence is associated with changes in the functioning of the body. The investigators want to determine if sleep apnea is associated with electrical disorders of the heart in patients with hypertrophic cardiomyopathy.

NCT ID: NCT03322319 Completed - Clinical trials for Left Ventricular Hypertrophy

Frequency of Cardiac Amyloidosis in the Caribbean's. (TEAM Amylose)

Start date: September 23, 2013
Phase: N/A
Study type: Interventional

The frequency of cardiac amyloidosis among patients presenting with a so-called left ventricular hypertrophy remains unknown. This problem is especially relevant in the Caribbean's, where an amyloidosis-prone mutation of transthyretin gene might be frequent.