Search clinical trials for: LP(a)

Total 474096 results

Purdue Pharma LP

Completed

To Determine the Fasting Bioequivalence of Reformulated OXY Tablets and Original OxyContin® (OXY) Tablets

Healthy

United States
AbbVie

Completed

A Phase 3b Study Evaluating the 24-Hour Intraocular Pressure Lowering Effect of Bimatoprost SR in Patients With Open-Angle Glaucoma or Ocular Hypertension

Ocular Hypertension | Open-Angle Glaucoma

United States
New York State Psychiatric Institute

Completed

A Stepped Care Model of Adolescent Depression Treatment in Primary Care (SCIPT-A)

Major Depressive Disorder | Dysthymia

United States
Medicrea, USA Corp.

Completed

Scoliosis Surgery Using the PASS® LP System

Idiopathic Scoliosis

United States
Skane University Hospital

Completed

Lactobacillus Plantarum 299v in Colon Surgery (Lp 299v)

Inflammation | Cell Proliferation | Bacterial Translocation

Sweden
Academisch Medisch Centrum - Universiteit van Amsterdam...

Unknown

Mechanism of Action of Ustekinumab in Psoriatic Arthritis (MoA anti-p40)

Arthritis, Psoriatic

Netherlands
Assistance Publique Hopitaux De Marseille

Unknown

Mechanical Characterization of Ascending Aorta in Patients With and Without Aortic Dissection

Acute Type A Dissection

France
Indiana University
National Institute on Alcohol Abuse and Alcoholism (NIAAA); Cedars-Sinai Medical...

Recruiting

SAMe Trial for Patients With Alcoholic Cirrhosis

Alcoholic Cirrhosis

United States
Allergan

Completed

A Study To Assess the Adverse Effects and Change in Condition of OnabotulinumtoxinA X Injection in Adult Participants With Forehead Lines

Forehead Lines

United States
University of Castilla-La Mancha

Completed

UHCDS a-tDCS Combined With Therapeutic Exercise in Fibromyalgia Patients

Fibromyalgia

Spain
Loma Linda University
Allergan

Completed

Assessment of the Effect of Botulinum Toxin in Extensor Digitorum Brevis Via Strain Gauge and Nerve Conduction Studies

Muscle Strength | Botulinum Toxins, Type A

United States
Akcea Therapeutics

Completed

Drug-drug Interaction Study to Evaluate the Effect of ISIS 681257 on Warfarin

Cardiovascular Diseases | Elevated Lipoprotein(a)

Canada
Akcea Therapeutics

Completed

Drug-drug Interaction Study to Evaluate the Effect of ISIS 681257 on Clopidogrel

Cardiovascular Diseases | Elevated Lipoprotein(a)

Canada
Rigshospitalet, Denmark
Groupe Hospitalier Pitie-Salpetriere

Completed

Effect of Bezafibrate on Muscle Metabolism in Patients With Fatty Acid Oxidation Defects (Bezafibrate)

Carnitine Palmitoyltransferase II Deficiency | Very Long Chain Acyl Coa Dehydrogenase Deficiency

Denmark
King Saud University

Completed

Extraction and Socket Preservation Before Implant Placement Using Freezed Dried Allograft (FDBA) and Platelet-Rich Fibrin in Smokers

A-PRF

Saudi Arabia
Chinese PLA General Hospital

Active, not recruiting

Microwave Ablation and Surgical Resection for Micropapillary Thyroid Carcinoma

Papillary Thyroid Carcinoma

China
Washington University School of Medicine
Genentech, Inc.

Completed

Safety and Effectiveness of Efalizumab to Treat Oral Lichen Planus

Lichen Planus, Oral

United States
Weill Medical College of Cornell University
National Institute of Mental Health (NIMH)

Completed

Reaching and Engaging Depressed Senior Center Clients (REDS II)

Depression in Old Age

United States
Shahid Beheshti University of Medical Sciences

Unknown

The Effect of Slanted Recession of Horizontal Muscle on Horizontal Strabismus With Abnormal Accommodative Convergence /Accommodation Ratio (AC/A)

Horizontal Strabismus With High AC/A Ratio

Iran, Islamic Republic of
Ellodi Pharmaceuticals, LP

Available

Expanded Access Protocol for Patients With Eosinophilic Esophagitis

Eosinophilic Esophagitis

United States
Ellodi Pharmaceuticals, LP

Completed

Efficacy and Safety APT-1011 in Adolescent Subjects With Eosinophilic Esophagitis (EoE) - A Sub-Study of the FLUTE-2 Trial (FLUTEEN)

Eosinophilic Esophagitis

Australia, United States
Purdue Pharma LP

Terminated

A Study to Evaluate the Analgesic Efficacy and Safety of VM902A in Subjects With Osteoarthritis (OA) of the Knee

Osteoarthritis Pain of the Knee

United States
Purdue Pharma LP

Withdrawn

Pharmacokinetics, Safety, and Efficacy of Intravenous Dosing of Buprenorphine in Pediatric Patients Who Require Opioid Analgesia for Acute Moderate to Severe Pain

Other Acute Postoperative Pain | Prolonged Endotracheal Intubation
Purdue Pharma LP

Completed

A Study of Oxycodone/Naloxone Controlled-release Tablets (OXN) to Assess Analgesic Efficacy and Management of Opioid-induced Constipation (OIC) in Opioid-experienced Subjects With Moderate to Severe Chronic Low Back Pain

Low Back Pain

United States
Purdue Pharma LP

Completed

The Safety and Efficacy of the Buprenorphine Transdermal Delivery System in Subjects With Chronic Low Back Pain.

Back Pain

United States
Purdue Pharma LP

Completed

Buprenorphine Transdermal System (BTDS) in Subjects w/Mod-sev Osteoarthritis (OA) Chronic Pain of Knee

Chronic Pain | Osteoarthritis of the Knee

United States
Purdue Pharma LP

Terminated

Safety and Efficacy of Buprenorphine Transdermal System (BTDS) in Subjects With Moderate to Severe Osteoarthritis Pain

Osteoarthritis

United States
Purdue Pharma LP

Completed

Buprenorphine Transdermal System (BTDS) in Subjects With Moderate to Severe Chronic Low Back Pain

Low Back Pain

United States
Purdue Pharma LP

Terminated

Buprenorphine Transdermal Patches (BTDS) in Subjects With Osteoarthritis Pain. Includes a 52-week Extension Phase.

Osteoarthritis

United States
Purdue Pharma LP

Terminated

Safety and Efficacy of Buprenorphine Transdermal System (BTDS) in Subjects With Moderate to Severe Low Back Pain

Back Pain Lower Back Chronic

United States
Purdue Pharma LP

Completed

Safety and Efficacy of Buprenorphine Transdermal System in Subjects With Moderate to Severe Osteoarthritis of Hip or Knee

Osteoarthritis

United States
Purdue Pharma LP

Completed

To Determine the Fed Bioequivalence of Reformulated OXY Tablets and Original OxyContin® (OXY) Tablets

Healthy

United States
Purdue Pharma LP

Completed

A Study to Determine the Fasting Bioequivalence of Reformulated OXY Tablets and Original OxyContin® (OXY) Tablets

Healthy

United States
Purdue Pharma LP

Completed

A Study to Determine the Fed Bioequivalence of Reformulated OXY Tablets and Original OxyContin® (OXY) Tablets

Healthy Volunteers

United States
Purdue Pharma LP

Terminated

Efficacy and Safety of Hydromorphone Hydrochloride Extended-Release Compared to Placebo in Subjects With Persistent Pain

Chronic Non-Malignant Pain

United States
Purdue Pharma LP

Completed

Safety and Efficacy of the Buprenorphine Transdermal Delivery System in Subjects With Osteoarthritis Pain.

Osteoarthritis

United States
University of Stellenbosch
Nestlè Nutrition Institute Africa; National Research Foundation (NRF) (RSA)

Completed

Effect of Lactobacillus Plantarum 299v on Symptoms of Irritable Bowel Syndrome

Irritable Bowel Syndrome

South Africa
Università degli Studi di Sassari
Dr. Dario Melodia; Dr. Milena Pisano; Dr. Aurea Lumbau; Prof. Silvio Mario Meloni; Prof. Edoardo Baldoni

Not yet recruiting

RCT GBR One Stages Comparing A-Oss and Autogenous Bone Versus A-Oss and LCR-A

Dental Implant | Guided Bone Regeneration

Italy
University of Castilla-La Mancha

Not yet recruiting

UHCDS a-tDCS + TE in Fibromyalgia Patients

Fibromyalgia

Spain
Children's Hospital Medical Center, Cincinnati

Completed

Comparing Auto-adjustable Positive Airway Pressure to Continuous Positive Airway Pressure in Children With Sleep Apnea

Obstructive Sleep Apnea

United States
Coopervision, Inc.

Completed

One Month Dispensing Study Comparing the Clinical Performance of the Comfilcon A Sphere Lenses Compared to Comfilcon A Asphere Lenses.

Myopia

United States
Johnson & Johnson Vision Care, Inc.

Completed

Dispensing Evaluation of New Daily Disposable Toric Soft Contact Lens.

Astigmatism

United States
Brigham and Women's Hospital

Not yet recruiting

Can Food Timing Reduce Your Diabetes Risk?

Dietary Habits

United States
Novartis Pharmaceuticals

Active, not recruiting

Study of Efficacy and Safety of Canakinumab in Japanese Patients With AOSD

Adult Onset Still's Disease

Japan
Duke University
David Grant U.S. Air Force Medical Center

Completed

Genetically Guided Statin Therapy

Hypercholesterolemia | Hydroxy-methylglutaryl-coenzyme A (HMG Co-A) Reductase Inhibitors Adverse Reaction

United States
Pierre Fabre Medicament

Completed

Exploratory Study of L.S.E.S.r. (LipidoSterolic Extract of Serenoa Repens)(PERMIXON® 160 mg Hard Capsule) Versus Tamsulosine LP Activity on Inflammation Biomarkers in Urinary Symptoms Related to BPH (Benign Prostatic Hyperplasia) (PERMIN)

Benign Prostatic Hyperplasia (BPH)

France, Spain, Portugal, Italy
Coopervision, Inc.

Completed

A Dispensing Clinical Trial of Comfilcon A Extended Range Multifocal Lenses

Presbyopia

United States
Coopervision, Inc.

Completed

A Dispensing Clinical Trial of Comfilcon A Extended Range Multifocal Lenses

Presbyopia

United States
Providence Health & Services
Microstein, LLC

Completed

Measurement of Relaxin Peptide in Multiple Sclerosis (MS)

Multiple Sclerosis, Relapsing-Remitting

United States
Haihe Biopharma Co., Ltd.
Shanghai Institute of Materia Medica, Chinese Academy of Sciences

Completed

Study of Simmitecan Hydrochloride in the Treatment of Advanced Solid Tumor

Advanced Solid Tumor

China

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