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Metabolic Responses of Dapagliflozin vs Sitagliptin in T2DM Patients Inadequately Controlled With Insulin Therapy PHASE4 The use of sodium glucose co-transporter 2 inhibitors (SGLT2i) has been ass...
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L2 Diabetes Centre, Queen Mary Hospital
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Diurnal Evaluation of OSA Upper Airway Collapsibility and Muscle Responsiveness N/A In the framework of pathophysiological trait in obstructive sleep apnea (OS...
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IRCCS Istituto Auxologico Italiano,Ospedale San Luca
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Ovarian Function With ENG Implant and UPA Use EARLY_PHASE1 Same day initiation of the etonogestrel (ENG) implant and oral ulipristal a...
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University of Utah
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A Post-marketing Surveillance to Assess Safety and Efficacy of Telostop Plus Tab. N/A Post-marketing surveillance of Telostop Plus Tab....
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Multiple Locations
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Enhancement of Stroke Rehabilitation With Levodopa PHASE3 Trial investigates the benefits and harms of Levodopa /Carbidopa 100/25mg c...
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Active Not Recruiting
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Kantonsspital Aarau, Neurozentrum
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Eye Cream 8-Week Efficacy Clinical Study NA To investigate efficacy on test cream \[Formula#899675 44A\] on female subj...
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Shanghai China-norm Quality Technical Service Co., Ltd., Shanghai, Shanghai 200072
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A Study of Orally Administered ZM-H1505R to Evaluate Safety, Tolerability and Pharmacokinetics After Single and Multiple Ascending Doses in Healthy Participants PHASE1 ZM-H1505R is an investigational drug developed by Shanghai Zhimeng Biopharm...
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Frontage Clinical Services
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Investigating Mild Cognitive Impairment in Patients And Controls With TD-fNIRS N/A The goal of the proposed observational, multi-site study is to use fNIRS ne...
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The Research Center of Southern California
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Ceftolozane-Tazobactam for Directed Treatment of Pseudomonas Aeruginosa Bacteremia and Pneumonia in Patients With Hematological Malignancies and Hematopoietic Stem Cell Transplantation PHASE4 The goal of this clinical trial is to learn whether the antibiotic ceftoloz...
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Weill Cornell Medicine
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Safety and Efficacy of Aliskiren in Pediatric Hypertensive Patients 6-17 Years of Age PHASE3 This double-blind 8 week study will evaluate dose response, efficacy (blood...
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Novartis Investigative Site
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