Search clinical trials for: Continuous lumbar plexus (LP) block analgesia

Total 25312 results

Janssen, LP

Completed

A 2-year Study of Patients With Schizophrenia Who Are Treated With Long-acting Injectable Risperidone.

Schizophrenia
Janssen, LP

Completed

Evaluation of the Efficacy and Safety of Risperidone Injections Given Once a Month to Adults With Schizophrenia or Schizoaffective Disorder

Psychotic Disorders | Schizophrenia
Janssen, LP

Completed

A Study of the Effectiveness and Safety of Risperidone Compared With Haloperidol and Placebo in Patients With Chronic Schizophrenia

Psychotic Disorders | Schizophrenia
Janssen, LP

Completed

A Study Comparing Three Strategies to Switch Patients With Schizophrenia or Schizoaffective Disorder to Risperidone After Unsuccessful Treatment With Olanzapine.

Schizophrenia | Schizoaffective Disorder
Boston Children's Hospital

Completed

Variability of Infant LP Insertion Site Based On Procedural Experience

Traumatic Lumbar Puncture

United States
University of Florida

Withdrawn

GPx Activity in Subjects With Aortic Stenosis Undergoing TAVR

Aortic Stenosis | Transcatheter Aortic Valve Replacement | Glutathione Peroxidase Activity

United States
Zhujiang Hospital

Recruiting

Effects of TRE With Lactobacillus Plantarum LP-KFY04 Supplementation on Overweight / Obese Individuals (TRELO)

Obesity

China
Seattle Children's Hospital
Life Sciences Development Fund

Unknown

Pediatric Lumbar Puncture Success Using the COMPASS

Lumbar Puncture

United States
AbbVie
PPD

Recruiting

Study to Evaluate Pregnancy Outcomes in Risankizumab Exposed Pregnancies Relative to Those Non-risankizumab Exposed Pregnancies in Women With FDA Approved Indications

Plaque Psoriasis | Crohn Disease | Psoriatic Arthritis | Other Conditions for Which Risankizumab is an FDA-approved Treatment

United States
Pfizer

Completed

Efficacy Of PF-05089771 In Treating Postoperative Dental Pain

Postoperative Dental Pain

United States
Novartis Pharmaceuticals

Completed

The Effects of a Single Intravenous Administration of Secukinumab (AIN457) or Canakinumab (ACZ885) in Dry Eye Patients

Dry Eye

United States
Kaizen Bioscience Co.

Recruiting

A Pharmacokinetic Study of LP-001 in Children With a Bacterial Infection

Bacterial Infections | Pediatric

United States
Universidade Estadual Paulista Júlio de Mesquita...

Recruiting

Administration of L. Paracasei 28.4 as an Adjunct to the Treatment of Periodontitis

Periodontitis

Brazil
Peking University

Recruiting

Safety and Efficacy of FOLFSIM Plus Toripalimab in the Treatment of Advanced or Metastatic Neuroendocrine Carcinoma

Neuroendocrine Carcinoma of the Bladder

China
Hospitales Universitarios Virgen del Rocío

Completed

Efficacy of Macroporous Polytetrafluoroethylene Mesh in Laparoscopic Hernia Repair (PTFE)

Hernia, Inguinal

Spain
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
Medical University of South Carolina
National Heart, Lung, and Blood Institute (NHLBI)

Completed

Effects of Behavioral Stress Reduction Programs on Blood Pressure in African American Youth

Heart Diseases | Cardiovascular Diseases | Hypertension

United States
Eli Lilly and Company

Completed

A Bioequivalence Study of Mirikizumab (LY3074828) in Healthy Participants

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
Shijiazhuang Junlebao Dairy Co., Ltd.
Atlantia Food Clinical Trials; Teagasc

Unknown

A Study on Efficacy of Feeding N1115 Probiotic Supplement to Young Children (N1115Baby)

Intestinal Growth of Young Children

Ireland
Ellodi Pharmaceuticals, LP

Active, not recruiting

24-Week Induction Study of APT-1011 in Adult Subjects With Eosinophilic Esophagitis (EoE) (FLUTE 3) (FLUTE-3)

Eosinophilic Esophagitis

United States, Canada
Purdue Pharma LP

Terminated

Safety and Tolerability Study of Adhansia XR® Extended-Release Capsules in Children

Attention Deficit/Hyperactivity Disorder

United States
Purdue Pharma LP

Withdrawn

Clinical Outcomes From Nalmefene (COINED)

Opioid Overdose
Ellodi Pharmaceuticals, LP

Completed

Efficacy and Safety APT-1011 in Adult Subjects With Eosinophilic Esophagitis (EoE) (FLUTE-2) (FLUTE-2)

Eosinophilic Esophagitis

United States, Australia, Spain
Bayer
Janssen, LP

Completed

Study to Gain Insights in Treatment Patterns and Outcomes in Patients With Atherosclerosis Prescribed to Xarelto in Combination With Acetylsalicylic Acid (XATOA)

Atherosclerosis

Germany, Argentina, Brazil, Canada, Denmark, Israel, Korea, Republic of, Lebanon, Luxembourg, Mexico, Norway, Russian Federation, Slovenia, Sweden, Switzerland, Thailand, United Arab Emirates, United Kingdom
Bayer
Janssen, LP

Completed

Study to Learn More About the Benefits and Side-effects of Drugs Rivaroxaban and Apixaban Compared to the Drug Warfarin for Stroke Prevention in Patients With Rapid and Irregular Heartbeat Which is Not Due to a Heart-valve Fault (Non-valvular Atrial Fibrillation) in the UK Routine Clinical Practice (SiERRA UK)

Atrial Fibrillation

United Kingdom
Purdue Pharma LP

Completed

Safety of Twice Daily Oxycodone Hydrochloride Controlled-release Tablets in Children With Moderate to Severe Malignant and/ or Nonmalignant Pain Requiring Opioids

Pain

United States, Israel, Spain, United Kingdom, Greece, Hungary, New Zealand, Romania
Purdue Pharma LP

Completed

The Effect of Buprenorphine Delivered by Buprenorphine Transdermal System (BTDS) at Doses up to 80 Micrograms/Hour (mcg/hr) and Naltrexone on Electrocardiogram (ECG) Intervals in Healthy Volunteers

ECG Effects

United States
Purdue Pharma LP

Completed

Experimental Biomarker Study for Pain Thresholds

Pain

Denmark
Purdue Pharma LP

Completed

An Open-label Study of Hydromorphone Oral Solution in Subjects Aged 28 Days to 16 Years for Postoperative Pain (Palladone)

Postoperative Pain

United States
Bayer
Janssen, LP

Completed

Real-Life Evidence on Stroke Prevention in SPAF (RELIEF)

Atrial Fibrillation (Prevention of Stroke)

Germany
Purdue Pharma LP

Completed

The Effect of Hydrocodone Bitartrate (HYD) Extended-Release Tablets on QT /QTc Intervals in Healthy Adult Subjects

Healthy

United States
Purdue Pharma LP

Terminated

An Analgesic Study to of V117957 for the Treatment of Postsurgical Pain Due to Third Molar Extraction

Postsurgical Pain Due to Third Molar Extraction

United States
Purdue Pharma LP

Completed

Analgesic Efficacy and Safety of V116517 in Subjects With Moderate to Severe Chronic Pain Due to Osteoarthritis (OA) of the Knee

Pain | Osteoarthritis, Knee

United States
Purdue Pharma LP

Completed

Safety of Buprenorphine Transdermal Systems in Subjects With Chronic Nonmalignant Pain - a 28-week Extension Study

Chronic Nonmalignant Pain

United States
Purdue Pharma LP

Terminated

Safety of Buprenorphine Transdermal System (BTDS) in Subjects With Acute Postoperative Pain After Total Knee Replacement

Postoperative Pain

United States
Purdue Pharma LP

Completed

Safety of BTDS in Subjects With Osteoarthritic (OA) Pain of Hip or Knee: A 6-Month Open-label Extension Phase

Osteoarthritis

United States
Purdue Pharma LP

Completed

Examine Plasma Concentrations of Buprenorphine Following Reapplication of Buprenorphine Transdermal System (BTDS) After Variable Application Site Rest Periods

Healthy

United States
Purdue Pharma LP

Completed

The Safety and Efficacy of the Buprenorphine Transdermal System (BTDS) in Subjects With Chronic Back Pain. (BP96-0604)

Back Pain

United States
Purdue Pharma LP

Completed

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

Healthy Volunteers

United States
Purdue Pharma LP

Completed

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

Healthy

United States
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
University of Georgia
Emory University

Not yet recruiting

Effect of DASH on HF Outcomes Heart Failure Status in Older Adults (DASH HF)

Heart Failure

United States
Academisch Medisch Centrum - Universiteit van Amsterdam...

Unknown

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

Arthritis, Psoriatic

Netherlands
Novartis Pharmaceuticals

Active, not recruiting

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

Adult Onset Still's Disease

Japan
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
Injeq Ltd

Completed

The First Puncture Success Rate of a Novel Injeq IQ-Tip™ System in Pediatric Lumbar Punctures (IQ-LP-03)

Lumbar Puncture

Finland
Bayer
Janssen, LP

Completed

Study to Gather Information About the Safety of Oral Anticoagulation Drugs and How Well These Drugs Work in Real World for Patients With Non-valvular Atrial Fibrillation (Irregularly Heart Beats Which is Not Caused by a Heart Valve Problem) (REATTAIN)

Atrial Fibrillation

Sweden

3

Subscribe