Clinical Trials on Sedation Method in Czechia

Total 26 results

Brno University Hospital

Completed

Establishment and Evaluation of a Post Caesarean Acute Pain Service (PCAPS) (PCAPS)

The Efficacy of Analgesic Methods After Caesarean Section

Czech Republic
Masaryk Hospital Krajská zdravotní a.s.

Completed

Effect of Midazolam and Dexmedetomidine on Heart Function - A Randomized MRI-based Study. (MRI)

Magnetic Resonance Imaging | Sedation | Cardiac Function

Czechia
Charles University, Czech Republic

Completed

Long-term tDCS Tinnitus Treatment

Tinnitus

Czechia
Charles University, Czech Republic
General University Hospital, Prague

Completed

Comparison of Surgical Conditions in Cesarean Section Under General Anesthesia With Deep Neuromuscular Blockade Versus Succinylcholine

Cesarean Section

Czechia
Charles University, Czech Republic
Military University Hospital, Prague

Recruiting

Optimization of Sedation Protocol for Endoscopic Procedures Using Impedance Ventilation Monitor.

Ventilatory Depression | Sedation Complication

Czechia
University of Erlangen-Nürnberg Medical School
Karolinska Institutet; University College, London; Erasmus Medical Center; Bambino... and other collaborators

Terminated

Efficacy, Safety and Pharmacokinetic Study of Intravenous Clonidine Versus Midazolam for Sedation in Paediatric Patients (CloSed1)

Sedation in Intensive Care

Spain, Sweden, Italy, Czechia, Estonia, Germany, Netherlands
Charles University, Czech Republic
The Jerzy Kukuczka Academy of Physical Education in Katowice

Enrolling by invitation

Physiotherapeutic Approach to Tinnitus

Tinnitus

Czechia
University Hospital, Motol

Completed

Manual Therapy Effects on Upper and Lower Esophageal Sphincter Pressures

Gastroesophageal Reflux Disease | Globus Pharyngeus

Czechia
Charles University, Czech Republic

Completed

Vestibular Function in Cochlear Implants

Vestibular Disorder | Deafness, Bilateral | Cochlear Trauma

Czechia
University Hospital Ostrava

Completed

Repetitive Transcranial Magnetic Stimulation for Chronic Subjective Tinnitus

Tinnitus, Subjective

Czechia
Strekin AG

Completed

Safety and Efficacy of STR001-IT and STR001-ER in Patients With SSHL

Acute Hearing Loss

Switzerland, Czechia, Germany
Brno University Hospital
University Hospital Olomouc; St. Anne's University Hospital Brno, Czech Republic and other collaborators

Completed

Modern Myorelaxation Procedure and Reversal of Neuromuscular Blockade With General Anesthesia for Caesarean Section (RocSugIO)

Caesarean Section | Pregnancy

Czech Republic
University Hospital Ostrava

Completed

Administration of Dexamethasone in PONV Prophylaxis in Children Undergoing Adenotomy

Snoring | Otitis | Hearing Loss | Nasal Obstruction | Apnea, Obstructive | Nasopharyngeal Obstruction

Czechia
Nordmark Arzneimittel GmbH & Co. KG
X-act Cologne Clinical Research GmbH; ClinSupport GmbH; MWI Medizinisches Wirtschaftsinstitut... and other collaborators

Completed

Efficacy, Safety, and Tolerability of Ancrod in Patients With Sudden Hearing Loss

Ear Diseases | Hearing Loss | Hearing Disorders | Deafness | Hearing Loss, Sensorineural

Czechia, Germany
AudioCure Pharma GmbH

Recruiting

Efficacy and Safety of AC102 Compared to Steroids in Adults With Idiopathic Sudden Sensorineural Hearing Loss (ISSNHL)

Hearing Loss, Sensorineural

Germany, Austria, Netherlands, Czechia, Poland, Serbia
Sensorion

Completed

Efficacy of SENS 401 in Subjects With Severe or Profound Sudden Sensorineural Hearing Loss (AUDIBLE-S)

Severe Sudden Sensorineural Hearing Loss

Israel, United Kingdom, France, Serbia, Bulgaria, Canada, Czechia, Germany, Slovakia, Turkey
Janssen Research & Development, LLC

Completed

54135419SUI3002: A Study to Evaluate the Efficacy and Safety of Intranasal Esketamine in Addition to Comprehensive Standard of Care for the Rapid Reduction of the Symptoms of Major Depressive Disorder, Including Suicidal Ideation, in Adult Participants Assessed to be at Imminent Risk for Suicide (Aspire II)

Depressive Disorder, Major

United States, Belgium, Canada, Poland, France, Spain, Brazil, Lithuania, Czechia, Austria, Argentina, Turkey
Pierre Fabre Medicament

Completed

Effect of V0251 in Acute Vertigo

Acute Vertigo

Spain, France, Germany, Czech Republic, Hungary
Merz Pharmaceuticals GmbH

Completed

Efficacy, Safety and Tolerability of Neramexane in Comparison to Placebo in Patients With Subjective Tinnitus

Subjective Tinnitus

Belgium, Czech Republic, France, Poland, South Africa, Netherlands
Novartis Pharmaceuticals

Completed

A Study of the Efficacy and Safety of Brolucizumab vs. Aflibercept in Patients With Visual Impairment Due to Diabetic Macular Edema (KITE)

Diabetic Macular Edema

Czechia, India, Russian Federation, Taiwan, Turkey, Lebanon, Denmark, Estonia, France, Germany, Hungary, Korea, Republic of, Latvia, Lithuania, Bulgaria, Norway, Belgium, Malaysia, Sweden, Slovakia, Singapore, Poland, Switzerland
Merz Pharmaceuticals GmbH

Terminated

Open-Label, Long-Term Treatment Study, to Assess the Long-Term Safety and Tolerability and Efficacy of Neramexane in Patients With Subjective Tinnitus (OLLTT)

Subjective Tinnitus

United States, United Kingdom, Poland, Austria, Belgium, Brazil, Czech Republic, France, Germany, Mexico, Netherlands, Portugal, South Africa, Spain
Novartis Pharmaceuticals

Completed

Efficacy and Safety of Ranibizumab Intravitreal Injections Versus Dexamethasone Intravitreal Implant in Patients With Branch Retinal Vein Occlusion (BRVO) (COMRADE-B)

Macular Edema | Visual Impairment | Branch Retinal Vein Occlusion

Germany, United Kingdom, Hungary, Poland, Czech Republic
Novartis Pharmaceuticals

Terminated

Assessing the Efficacy and Safety of Brolucizumab Versus Aflibercept in Patients With Visual Impairment Due to Macular Edema Secondary to Branch Retinal Vein Occlusion (RAPTOR)

Branch Retinal Vein Occlusion

China, Austria, Czechia, Russian Federation, Taiwan, United Kingdom, Canada, Japan, United States, France, Israel, Germany, Italy, Hong Kong, Spain, Denmark, Slovakia, Puerto Rico, Switzerland
Novartis Pharmaceuticals

Completed

Efficacy and Safety of Ranibizumab in Two "Treat and Extend" Treatment Algorithms Versus Ranibizumab As Needed in Patients With Macular Edema and Visual Impairment Secondary to Diabetes Mellitus (RETAIN)

Diabetic Macular Edema

Belgium, United Kingdom, Netherlands, Ireland, Switzerland, Italy, Hungary, France, Spain, Portugal, Poland, Czech Republic, Greece
Novartis Pharmaceuticals

Terminated

Assessing the Efficacy and Safety of Brolucizumab Versus Aflibercept in Patients With Visual Impairment Due to Macular Edema Secondary to Central Retinal Vein Occlusion (RAVEN)

Central Retinal Vein Occlusion

China, Czechia, Germany, Russian Federation, Turkey, United States, Australia, Canada, Spain, United Kingdom, Thailand, Israel, Netherlands, Italy, Hungary, France, Greece, Puerto Rico, Malaysia, Japan
Novartis Pharmaceuticals

Completed

Ranibizumab Intravitreal Injections in Patients With Visual Impairment Due to Macular Edema Secondary to Central Retinal Vein Occlusion (CRYSTAL)

Central Retinal Vein Occlusion | Macular Edema

Greece, Hungary, Turkey, Australia, Austria, Netherlands, United Kingdom, Italy, Spain, Ireland, Portugal, Slovakia, Canada, Switzerland, Czech Republic, Poland, Denmark, Sweden

Clinical Trials on Sedation Method in Czechia

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