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Hypertrophy clinical trials

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NCT ID: NCT02674958 Terminated - Clinical trials for Hypertrophic Obstructive Cardiomyopathy

Mobilization of Endothelial Progenitor Cells and Aspirin

TROPHIC 3
Start date: May 2016
Phase: Phase 3
Study type: Interventional

Aspirin at doses used during acute myocardial infarction may inhibit the mobilization of endothelial progenitor cells (EPCs).

NCT ID: NCT02618447 Terminated - Liver Cancer Clinical Trials

4D Phase Contrast MR: Hypertrophy in Liver Cancer

Start date: August 5, 2014
Phase: N/A
Study type: Interventional

The investigators hypothesize that 4Dimensional Phase Contrast Magnetic Resonance Angiography (4D PC MRA) evaluation of portal venous flow predicts underlying liver function and hypertrophic potential in patients with liver cancer presenting for portal vein embolization (PVE). 4D PC MRA may provide a non-invasive measure of liver function that could help determine which patients could safely and successfully undergo PVE and subsequent resection of tumor. By comparing 4D PC MRA results with invasive catheter measurements the investigators will validate the flow findings. Further regression/correlation analysis with functional measures of the liver (HIDA scans), volumetrics, Doppler flow analysis, histology, and outcomes will help the investigators to determine the ability of 4D PC MRA to predict functional status and hypertrophic potential of the liver prior to PVE and hepatectomy allowing for better patient selection and reduced morbidity/mortality.

NCT ID: NCT02291237 Terminated - Clinical trials for Hypertrophic Cardiomyopathy

Effect of Eleclazine (GS-6615) on Exercise Capacity in Subjects With Symptomatic Hypertrophic Cardiomyopathy

LIBERTY-HCM
Start date: February 5, 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The primary objective of this study was to evaluate the effect of eleclazine (GS-6615) on exercise capacity as measured by Peak oxygen uptake (VO2) achieved during cardiopulmonary exercise testing (CPET), in participants with symptomatic hypertrophic cardiomyopathy (HCM).

NCT ID: NCT02205476 Terminated - Clinical trials for Hypertrophic Scars Resulting From Prior Breast Scar Revision Surgery

A Phase 2 Extension Study To Enroll Subjects Who Were Enrolled In B5301001 Study

Start date: December 2014
Phase: Phase 2
Study type: Interventional

Study is a multicenter, two-part, open-label phase II study in adults, evaluating the safety and long-term efficacy of PF-06473871 one year after surgical revision and treatment with PF-06473871.

NCT ID: NCT02162433 Terminated - Clinical trials for Obstructive Sleep Apnea

The Effect of Dexmedetomidine on Airway Complications After Deep or Awake Extubation

Start date: March 2015
Phase: Phase 4
Study type: Interventional

The investigators aim to investigate the effect of dexmedetomidine on the perioperative respiratory complications in this patient population undergoing both awake and deep tracheal extubation.

NCT ID: NCT01889992 Terminated - Immunosuppression Clinical Trials

Cardiac Allograft Remodeling and Effects of Sirolimus

CAR
Start date: April 24, 2013
Phase: Phase 1
Study type: Interventional

Cardiac allograft remodeling causes poor quality of life, allograft failure and increased mortality after heart transplantation. Risk factors for cardiac allograft remodeling and its progression are poorly defined and there is a need for effective interventions.This is a multi-factorial phenomenon, associated with various immunological and non-immunological factors. Animal studies suggest M-TOR inhibition attenuates cardiac allograft remodeling secondary to down-regulation of M-TOR downstream targets and increased autophagy. There is a paucity of data regarding effect of Sirolimus, a M-TOR inhibitor, on human heart remodeling. This aim of the proposal to identify the prevalence of cardiac allograft remodeling on current immunosuppressive strategies and determine risk factors for its development. It will also identify molecular pathways associated with cardiac allograft remodeling and determine the impact of Sirolimus on these pathways.

NCT ID: NCT01574885 Terminated - Clinical trials for Sleep Apnea, Obstructive

Efficacy of Aerosal® in the Treatment of Sub-Obstructive Adenotonsillar Hypertrophy and Related Diseases

Start date: February 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy of Aerosal® compared to a placebo treatment in the prognosis of sub-obstructive adenotonsillar hypertrophy present for at least six months.

NCT ID: NCT01564407 Terminated - Burn Scar Clinical Trials

A Clinical Study of Allogeneic Human Dermal Fibroblasts for Remodeling Scar Contractures

Start date: January 2011
Phase: Phase 1/Phase 2
Study type: Interventional

The primary objective of this study is to evaluate the safety of ICX-RHY-013 in the treatment of stable, restrictive scars in subjects who have suffered a burn injury. Evaluation will be achieved through regular assessment of adverse events, vital signs, blood work monitoring and laboratory analysis cellular properties of the scar through biopsy. The secondary objectives of this study are to evaluate improvement in symptoms of scars including reduced pain, discomfort and itching, improvement in mobility and daily function, improvement in appearance and scar texture.

NCT ID: NCT01427374 Terminated - Clinical trials for End Stage Renal Disease

Risk Factors for Coronary Artery Calcification and Left Ventricular Hypertrophy in Hemodialysis Patients

Start date: May 2011
Phase:
Study type: Observational

Individuals with kidney disease are at a higher risk for heart and vascular diseases, including heart attacks and strokes, than those with normal kidney function. The purpose of this research study is to collect information on the causes, complications and treatment of kidney disease. Patient characteristics, comorbid diseases and laboratory markers used in routine practice, as well as novel biochemical markers and genetic data will be collected to examine relationships between biochemical and genetic markers and cardiovascular risk. Information on the health history of incident hemodialysis and peritoneal dialysis patients will be captured using structured patient interviews and review of medical records. Blood and urine specimens will be collected at the time of dialysis initiation and stored in order to perform novel biochemical and genetic assays in the future. The overall goal of the CKDCS/LUCID study is improve understanding of cardiac-associated risks and to improve treatment in patients with kidney disease. A cardiac imaging substudy will be performed in a subset of patients enrolled. The goals of the substudy are to examine whether the risks of developing common cardiac-related complications (coronary artery calcification [CAC] and left ventricular hypertrophy [LVH]) are associated with certain medications taken by individuals on dialysis and whether these risks are modified by a genotypic predisposition.

NCT ID: NCT01349205 Terminated - Clinical trials for Obstructive Sleep Apnea

Caffeine in Children With Obstructive Sleep Apnea, Dose Response Study

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

The aim of this study is to evaluate whether a smaller dose of caffeine sodium benzoate 10 mg/kg IV is as effective as 20 mg/kg IV in decreasing the number of children who develop post extubation adverse upper airway respiratory events compared to placebo.