Search clinical trials for: Arndt® blocker

Total 24821 results

Imam Abdulrahman Bin Faisal University

Completed

Selective Lobar Blockade and Bronchial Blockers

One Lung Ventilation | Elective Thoracic Surgery

Saudi Arabia
Istanbul University

Not yet recruiting

Comparing Arndt and Tappa Endobronchial Blocker During Pediatric One Lung Ventilation

Lung Diseases

Turkey
Mahidol University

Completed

The Use of LMA-Proseal and Endobronchial Blocker for One Lung Anesthesia, Case Series

One-lung Ventilation | Anesthetic Technique

Thailand
University of British Columbia

Recruiting

A Novel Method of Lung Isolation Compared With Standard Methods in a Model of Massive Pulmonary Hemorrhage (BloodyBlocker)

Pulmonary Hemorrhage

Canada
Javier H Campos

Completed

One-Lung Ventilation in the Morbidly Obese Patient: Comparison of Double Lumen Versus Bronchial Blockers

Obesity

United States
Otto-von-Guericke University Magdeburg

Completed

Lung Isolation in Thoracic Surgery - a Randomized Trial Comparing the VivaSight™ EB Endobronchial Blocker With Established Devices

One-Lung Ventilation | Lung Separation Techniques
Eurofarma Laboratorios S.A.

Terminated

Safety and Efficacy of Furosemide 40mg + Amiloride Hydrochloride 10mg to Reduct Edema

Congestive Heart Failure

Brazil
University of Baghdad

Completed

Sperms Activation by Direct Electrical Shocks on Testis in Infertile Males

Infertility

Iraq
Bial - Portela C S.A.

Completed

Bioequivalence of Two Different Sources of Eslicarbazepine Acetate

Epilepsy
Yuhan Corporation

Completed

High-Dose Statin Combined With Telmisartan vs Amlodipine on Glucose Metabolism in ASCVD Patients With IFG and Hypertension

Hypertension | Impaired Fasting Glucose | ASCVD

Korea, Republic of
KRKA
University Medical Centre Ljubljana; Clinres Farmacija d.o.o.

Completed

Management of Newly Diagnosed and Uncontrolled Hypertension With Fixed-Dose Combination of Perindopril/Amlodipine and Perindopril/Indapamide/Amlodipine (PRECIOUS)

Hypertension

Armenia, Croatia, Hungary, Poland, Russian Federation, Serbia, Slovenia
Nantes University Hospital

Unknown

Medico-economic Study of Patient Matched Cutting Blocks (Ancillary) MyKnee ® LBS During Knee Arthroplasty GMK ®.

Osteoarthritis

France
Yonsei University

Completed

The Effect of Deep Neuromuscular Block on the Perioperative Stress Response Reduction and Postoperative Recovery Enhancement in Robot-assisted Stomach Cancer Surgery

Stomach Cancer

Korea, Republic of
Nantes University Hospital

Active, not recruiting

Medico-economic Interest of the Patient Matched Cutting Blocks (Ancillary) MyKnee ® LBS During the Poses of Complete Prosthesis of Knee GMK ®. Multicentric, Prospective, Controlled, Opened, Randomised Study About a Medical Device. (My Knee) (MY Knee)

Osteoarthritis

France
Biogen
Acorda Therapeutics

Completed

A Pharmacokinetics (PK) and Safety Study of Oral Fampridine-PR 10 mg in Chinese, Japanese, and Caucasian Adult Healthy Volunteers

Healthy

Hong Kong, Australia
AbbVie

Completed

A Study to Evaluate Satisfaction in Adult Participants With the Aesthetics of the Periorbital Area After JUVÉDERM® Fillers and BOTOX®/VISTABEL® Injections

Facial Corrections | Facial Lines

Australia, Belgium
Dong-A ST Co., Ltd.

Completed

The Efficacy and Safety of OROSARTAN® Versus CODIOVAN® in Patients With Essential Hypertension Uncontrolled With Monotherapy

Hypertension

Korea, Republic of
University Health Network, Toronto

Completed

Suprascapular and Axillary Blocks Versus Interscalene Block for Shoulder Surgery (PASS)

Shoulder Pain

Canada
Bial - Portela C S.A.

Completed

Effect of Repeat Administration of Eslicarbazepine Acetate on the Pharmacokinetics of a Combined Oral Contraceptive

Partial Epilepsy

Portugal
University College Hospital Galway

Recruiting

A Comparison of Two Regional Techniques for Bariatric Sleeve Gastrectomy

Weight Loss | Surgery | Bariatric Surgery Candidate

Ireland
Allergan

Completed

A Safety and Efficacy Study of JUVÉDERM® VOLIFT® With Lidocaine and Restylane® for Nasolabial Folds in Chinese Adults

Nasolabial Fold

China
Ohio State University
Gilead Sciences

Completed

Study of Ranolazine in Myotonia Congenita, Paramyotonia Congenita and Myotonic Dystrophy Type 1

Myotonic Dystrophy 1 | Myotonia Congenita | Paramyotonia Congenita

United States
UCB Pharma

Completed

Trial to Assess Optimized Dosage of Lacosamide as add-on Therapy in Patients With Partial Onset Seizure (SELF)

Partial Epilepsies

France
Dong-A Pharmaceutical Co., Ltd.
Dong-A ST Co., Ltd.

Unknown

Pharmacokinetic/Pharmacodynamic & Safety Study of G3041 and SEVIKAR® Tablet in Healthy Adult Volunteers

Healthy Adult Volunteers
UCB BIOSCIENCES, Inc.

Completed

Open-Label Extension Study to Assess the Safety and Seizure Frequency Associated With Lacosamide for Primary Generalized Tonic-Clonic Seizures in Subjects With Epilepsy

Epilepsy

United States
Medy-Tox

Completed

Neuramis® Volume Lidocaine Treatment in Patients With Loss of Mid-face Volume

Aging

Korea, Republic of
UCB Pharma

Completed

Post-Authorization Safety Study to Assess the Safety of Vimpat as add-on Therapy in Patients With Partial-onset Seizures (PASS)

Epilepsies, Partial

France, Germany, United Kingdom, Spain, Netherlands
UCB BIOSCIENCES, Inc.

Completed

Open-Label Study to Assess Lacosamide Safety as Add-on Therapy for Primary Generalized Tonic-Clonic Seizures in Subjects With Epilepsy

Epilepsy

United States
Teoxane SA

Completed

TEOSYAL® PureSense Redensity [I] Injection Using MicronJet® Needle in the Treatment of Crow's Feet Wrinkles

Crow's Feet Wrinkles

Switzerland
UCB BIOSCIENCES, Inc.

Completed

An Open-Label Study to Determine Safety , Tolerability, and Efficacy of Oral Lacosamide in Children With Epilepsy

Epilepsy

United States, Belgium, China, France, Germany, Hungary, Italy, Japan, Mexico, Poland, Ukraine
UCB Pharma

Completed

To Evaluate the Pharmacokinetics and Safety/Tolerability of Lacosamide in 3 Dosages in Healthy Male Korean Subjects

Epilepsy
Smiths Medical, ASD, Inc.

Unknown

Prospective Post-market Evaluation of an Echogenic Catheter (EchoCath)

Peripheral Nerve Block Procedure

United Kingdom
UCB Pharma

Completed

Belgian Drug-utilization Study to Evaluate the Use of VIMPAT® as Adjunctive Treatment of Partial Onset Seizures in Subjects Aged 16 and Older

Seizures

Belgium
Brazilan Center for Studies in Dermatology

Completed

Use Of Three Commercial Preparations Of Injectable Hyaluronic Acid In Hands Rejuvenation

Injuries to the Wrist and Hand

Brazil
Vitebsk Regional Clinical Hospital

Unknown

Comparative Effectiveness of the Minimally Invasive Coronary Artery Bypass Grafting

Myocardial Ischemia | Heart Diseases | Coronary Artery Disease

Belarus
Teoxane SA
ethica Clinical Research Inc.

Completed

TEOSYAL® RHA Global Action, TEOSYAL® RHA Deep Lines, and Juvéderm® Ultra XC for the Correction of Nasolabial Folds

Nasolabial Folds, Wrinkles

United States
Bio2 Technologies
MCRA

Terminated

Novum Vitrium® Cervical Cage in Anterior Cervical Discectomy and Fusion

Symptomatic Cervical Disc Disease

United States
Mylan Pharmaceuticals Inc

Completed

Steady-State Study of Extended Phenytoin Sodium Capsules 100 mg and Dilantin® Kapseals® 100 mg

Healthy

United States
Novartis Pharmaceuticals

Terminated

Evaluation of Exercise Treadmill Test (ETT) Indices in Participants With Cardiovascular Disease

Atherosclerotic Coronary Vascular Disease

United States
Northwell Health
Gilead Sciences

Terminated

Randomized Double Blind Control Trial on Effects of Ranolazine on New Onset Atrial Fibrillation

Hemorrhage | Ventricular Tachycardia | Atrial Fibrillation New Onset | Prolonged QTc Interval | Medical Care; Complications, Late Effect of Complications

United States
Gilead Sciences

Completed

Exploratory Study to Access the Metabolic Effects of Ranolazine in Subjects With Type 2 Diabetes Mellitus When Added to Ongoing Non-insulin Antidiabetic Therapy

Diabetes Mellitus, Type 2

United States
Chiesi Farmaceutici S.p.A.

Completed

Pilot Pharmacokinetic Clenil Study With AeroChamber Plus™ or Volumatic™ Spacer Devices

Asthma

United Kingdom
Biogen

Completed

Exploratory Study to Assess the Effect of Fampridine (BIIB041) on Walking Ability and Balance in Participants With Multiple Sclerosis. (MOBILE)

Multiple Sclerosis

Sweden, United Kingdom, Netherlands, Belgium, Canada, Italy
UCB Pharma

Completed

An Open-label follow-on Trial to Assess the Long-term Safety and Efficacy of Oral SPM 927 in Subjects With Diabetic Neuropathy

Painful Diabetic Neuropathy
UCB Pharma

Completed

A Trial to Investigate Safety and Efficacy of SPM927 in Painful Diabetic Neuropathy

Painful Diabetic Neuropathy
UCB Pharma

Completed

A Multi-Centre, Randomized, Double-Blind, Placebo Controlled Pilot Trial to Assess the Efficacy, Safety, and Tolerability of SPM 927 in Subjects With Postherpetic Neuralgia (PHN).

Postherpetic Neuralgia
UCB Pharma

Completed

eValuation of the Efficacy and toleRability of Vimpat When Added to lEvetiracetam (VERVE)

Epilepsy

United States, Australia, Bulgaria, Denmark, France, Germany, Romania, Spain, Sweden
Gilead Sciences

Completed

Type 2 Diabetes Evaluation of Ranolazine in Subjects With Chronic Stable Angina (TERISA)

Coronary Artery Disease | Type 2 Diabetes Mellitus | Angina Pectoris

Canada, Slovenia, United States, Israel, Germany, Georgia, Russian Federation, Czech Republic, Belarus, Bulgaria, Poland, Serbia, Slovakia, Ukraine
Uppsala University Hospital
Swedish Heart Lung Foundation

Unknown

Catheter Ablation Compared With Pharmacological Therapy for Atrial Fibrillation (CAPTAF Trial) (CAPTAF)

Quality of Life | Atrial Fibrillation

Sweden
Allergan
TARIS Biomedical, Inc.

Terminated

Double-Blind Placebo Controlled Study of Safety,Tolerability, and Efficacy of LiRIS® in Women With Interstitial Cystitis

Interstitial Cystitis

United States, Canada

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