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7 studies found for:    CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 2
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Rank Status Study
1 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
2 Completed Comparison of Reduced Cuff-pressure of the Laryngeal Tube Under General Anesthesia
Condition: Airway Morbidity
Intervention: Device: Reduce Cuff pressure
3 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
4 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
5 Recruiting Open-Label Study of Perhexiline in Patients With Hypertrophic Cardiomyopathy and Moderate to Severe Heart Failure
Conditions: Cardiomyopathy, Hypertrophic;   Cardiomyopathy, Hypertrophic, Familial
Intervention: Drug: Perhexiline
6 Terminated Effect of Eleclazine (GS-6615) on Exercise Capacity in Subjects With Symptomatic Hypertrophic Cardiomyopathy
Condition: Hypertrophic Cardiomyopathy
Interventions: Drug: Eleclazine;   Drug: Placebo
7 Available Compassionate Use of Triheptanoin (C7) for Inherited Disorders of Energy Metabolism
Conditions: Very Long-chain acylCoA Dehydrogenase (VLCAD) Deficiency;   Carnitine Palmitoyltransferase Deficiencies (CPT1, CPT2);   Mitochondrial Trifunctional Protein Deficiency;   Long-chain Hydroxyacyl-CoA Dehydrogenase Deficiency;   Glycogen Storage Disorders;   Pyruvate Carboxylase Deficiency Disease;   ACYL-CoA DEHYDROGENASE FAMILY, MEMBER 9, DEFICIENCY of;   Barth Syndrome
Intervention: Drug: triheptanoin

Study has passed its completion date and status has not been verified in more than two years.