4 studies found for:    CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 2
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Rank Status Study
1 Completed Wean Obese Study : Determination of the Optimal Spontaneous Breathing Trial for Obese Patient
Conditions: Obesity;   Respiratory Failure;   PSV 7cmH2O PEEP 7cmH2O;   PSV 7 cmH2O PEEP 0 cmH20;   CPAP 7 cmH2O;   PSV 0 cmH20 PEEP 0 cmH2O;   T-Tube;   Post-extubation in Spontaneous Breathing and/or in NIV
Intervention: Procedure: Spontaneous breathing trial
2 Completed Intraoperative Protective Ventilation in Abdominal Surgery (IMPROVE Study)
Conditions: Protective Lung Ventilation Using:;   Low Tidal Volume (6-8 mL/kg Predicted Body Weight);   PEEP of 6-8 cmH2O;   Intraoperative RMs
Intervention: Other: Abdominal surgery
3 Completed 10cmH2O Peep Application and Cerebral Oxygenation in Laparoscopic Surgery: a Comparative Study With Invos and Foresight Devices
Condition: Laparoscopic Cholecystectomy
Interventions: Device: FORESİGHT cerebral oxygen monitor and INVOS cerebral oxygen monitor;   Device: FORESIGHT and INVOS monitor
4 Recruiting Congenital Muscle Disease Study of Patient and Family Reported Medical Information
Conditions: Muscular Dystrophy;   Congenital Muscular Dystrophy;   Fukutin-related Protein Gene;   Limb Girdle;   FKRP Gene;   Childhood Onset LGMD;   Adult Onset LGMD;   POMT1;   POMT2;   POMGnT1;   LARGE;   Alpha Dystroglycan;   Dystroglycanopathy;   Centronuclear;   Multiminicore;   Multicore;   Minicore;   Congenital Fiber Type Disproportion;   Myotubular;   Nemaline;   Congenital Myopathy;   Neuromuscular;   Rigid Spine;   Phenotype-Genotype Correlation;   Cough Assisted Device;   Neuromuscular Disease;   Respiratory Exacerbation;   Invasive Ventilation;   Chest Physiotherapy;   Congenital Myopathies;   Genetic Mutations;   Hypertrophic Cardiomyopathy;   Wheelchair Use;   Cataract;   Opthalmoplegia;   Ullrich Congenital Muscular Dystrophy;   Intermediate Collagen VI Myopathy;   Laminin Alpha 2 Related Congenital Muscular Dystrophy;   MDC1A;   Merosin Deficient Congenital Muscular Dystrophy;   Congenital Muscular Dystrophy Undiagnosed;   Congenital Muscular Dystrophy Merosin Positive;   Walker Warburg Syndrome;   Muscle Eye Brain Disease;   Fukuyama;   Integrin Alpha 7 Deficiency;   Integrin Alpha 9 Deficiency;   Laminopathy;   Lamin AC;   SEPN 1 Related Myopathies;   Bethlem Myopathy;   Dystroglycanopathies;   LGMD2K;   LGMD2I;   LGMD2L;   LGMD2N;   Actin Aggregation Myopathy;   Cap Disease;   Central Core Disease;   Centronuclear Myopathy;   Core Rod Myopathy;   Hyaline Body Myopathy;   Multiminicore Myopathy;   Myotubular Myopathy;   Nemaline Myopathy;   Tubular Aggregate Myopathy;   Zebra Body Disease Myopathy;   Congenital Myopathy Other;   Reducing Body Myopathy;   Sarcotubular Myopathy;   Spheroid Body Myopathy
Intervention:

Indicates status has not been verified in more than two years