- ICH GCP
- US Clinical Trials Registry
- Search trials
Clinical Trials on Spasticity of the Upper and Lower Limb Due to Cerebral Causes in New Zealand
Total 12 results
-
Merz Pharmaceuticals GmbHCompletedSpasticity of the Upper and Lower Limb Due to Cerebral CausesGermany, United States, Canada, France, Italy, Norway, Portugal, Spain
-
Merz Pharmaceuticals GmbHRecruitingLower Limb or Combined Lower Limb and Upper Limb Spasticity Due to Stroke or Traumatic Brain InjuryUnited States, Belgium, Czechia, France, Germany, Italy, Poland, Spain, Switzerland, United Kingdom, Australia, Hungary, Norway, Slovakia, Ukraine, Russian Federation
-
Merz Pharmaceuticals GmbHCompletedPost-stroke Spasticity of the Upper LimbPoland, United States, Czech Republic, Germany, Hungary, India, Russian Federation
-
Merz Pharmaceuticals GmbHCompletedPost-stroke Spasticity of the Lower LimbGermany, Poland, Spain, United States, Czech Republic, Russian Federation, Canada, France, Italy
-
Northwell HealthTerminatedStroke | Stroke Sequelae | Hemiparesis | Hemiplegia, Spastic | CVA | Spasticity as Sequela of Stroke | Upper Limb HypertoniaUnited States
-
Merz Pharmaceuticals GmbHCompletedEssential Tremor of the Upper LimbUnited States, Canada, Poland
-
Tris Pharma, Inc.Forest LaboratoriesCompletedModerate to Severe Chronic Pain Due to Osteoarthritis of the KneeUnited States
-
Merz Pharmaceuticals GmbHCompleted
-
MeiraGTx, LLCRecruitingGrade 2 and 3 Late Xerostomia Caused by Radiotherapy for Cancers of the Upper Aerodigestive Tract, Excluding the Parotid GlandsUnited States, Canada
-
Helius Medical IncRecruitingGait Impairment Due to Mild/Moderate Multiple Sclerosis (MS)United States
-
Ruhr University of BochumUnknownComplex Regional Pain Syndrome Type I of the Upper LimbGermany
-
National Heart, Lung, and Blood Institute (NHLBI)National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)CompletedMarfan Syndrome | Turner Syndrome | Ehlers-Danlos Syndrome | Loeys-Dietz Syndrome | Shprintzen-Goldberg Syndrome | FBN1, TGFBR1, TGFBR2, ACTA2 or MYH11 Genetic Mutation | Bicuspid Aortic Valve Without Known Family History | Bicuspid Aortic Valve With Family History | Bicuspid Aortic Valve With Coarctation and other conditionsUnited States