Search clinical trials for: Intravenous diclofenac sodium (DIC075V)

Total 713 results

Javelin Pharmaceuticals

Completed

Study to Compare the Pharmacokinetics of IV Diclofenac Sodium (2 Doses)Versus Oral Diclofenac Potassium

Healthy

United States
Pfizer

Completed

An Open-Label Safety Study Of DIC075V (Intravenous Diclofenac Sodium) In Patients With Acute Post-Operative Pain

Pain, Postoperative

United States
Javelin Pharmaceuticals

Completed

Study to Assess Effects of Age, Weight, and Body Composition on the Pharmacokinetics of IV Diclofenac Sodium (DFC-PK-008)

Healthy

United States
Javelin Pharmaceuticals

Completed

Efficacy and Safety of IV Diclofenac (DIC075V) for Pain After Abdominal or Pelvic Surgery

Pain, Postoperative

United States
Javelin Pharmaceuticals

Completed

Platelet Function and Safety After IV and Oral Diclofenac, IV Ketorolac and Oral Aspirin in Adult Volunteers

Healthy

United States
Rush University Medical Center

Recruiting

Aquacel Hypersensitivity Dressing in TJAs

Contact Allergic Dermatitis | Adverse Skin Reaction

United States
Azienda Ospedaliera Città della Salute e della...

Completed

Acute Neuroendocrine Response to Intravenous Infusion of Diclofenac Sodium

Hypopituitarism

Italy
University of Monastir

Completed

Treatment of Renal Colic in the Emergency Department: Comparison Between Magnesium Sulfate and Lidocaine.

Renal Colic

Tunisia
Mallinckrodt

Completed

Pharmacokinetics, Bioavailability and Safety of PENNSAID® Gel

Pain

United States
University Hospital Rijeka

Completed

Diclophenac Versus Placebo for Pain Control in Diagnostic Colonoscopy

Anemia

Croatia
Boehringer Ingelheim

Completed

Comparison of the Bioavailability of Diclofenac in a Combination Product (Diclofenac 2% + Capsaicin 0.075% Topical Gel) With Two Diclofenac Only Products, Diclofenac Mono Gel 2% and Voltarol® 12 Hour Emulgel 2.32% Gel, in Healthy Volunteers

Healthy

South Africa
Sheba Medical Center
Tel Aviv University

Completed

Intravenous Sodium Bicarbonate Verifies Intravenous Position of Catheters in Children

Verifying the Correct Position of Intravenous Catheters

Israel
Tularik

Unknown

Study of T900607-Sodium in Chemotherapy Naive Patients With Hepatocellular Carcinoma.

Hepatocellular Carcinoma

United States, China
Tularik

Terminated

Study of T900607-Sodium in Previously Treated Patients With Non-Hodgkin's Lymphoma.

Non-Hodgkin's Lymphoma

United States
BDD Pharma Ltd
Drug Delivery International Ltd

Completed

Delayed Release Diclofenac Sodium Formulation vs Voltaren®

Pain

United Kingdom
Tularik

Unknown

Study of T900607-Sodium in Previously Treated Patients With Ovarian Cancer.

Ovarian Neoplasms

United States
Tularik

Suspended

Study of T900607-Sodium in Subjects With Previously Treated Gastric Cancer or Adenocarcinoma of the Esophagus

Gastric Cancer | Esophageal Neoplasms

United States
Fidia Farmaceutici s.p.a.

Completed

Comparative Bioavailability and Local Tolerability of Two Topical Diclofenac Plasters Applied Once and Twice a Day

Bioequivalence Study

Italy
Panineeya Mahavidyalaya Institute of Dental Sciences...

Completed

A Comparative Evaluation of Diclofenac Sodium Transdermal Patch, Oral Diclofenac Sodium With Intramuscular Injections of Diclofenac Sodium in Patients Suffering From Oral Pain

Orofacial Pain

India
Amneal Pharmaceuticals, LLC
Sristek Clinical Research Solutions Limited

Completed

Study Comparing a Generic Diclofenac Sodium Topical Gel, 1% to Voltaren in the Treatment of Subjects With Osteoarthritis of the Knee

Osteoarthritis

India
Zambon SpA
Cross Research S.A.

Completed

Drug Interaction Study of Safinamide and a BCRP Substrate, Diclofenac, Concomitantly Administered to Healthy Volunteers

Healthy

Switzerland
The Western Pennsylvania Hospital
West Penn Allegheny Health System

Withdrawn

Oral Versus Intravenous Hydration to Prevent Contrast Induced Nephropathy (HYDRATE)

Contrast Induced Nephropathy

United States
Noven Pharmaceuticals, Inc.

Completed

A 4-week Study to Evaluate the Efficacy and Safety of HP-5000 in Subjects With Knee Osteoarthritis (HP-5000)

Osteoarthritis of the Knee

United States
Taro Pharmaceuticals USA

Completed

A Study Comparing Diclofenac Sodium Gel 3% to Solaraze® Gel 3% in the Treatment of Actinic Keratosis

Actinic Keratosis
Mylan Pharmaceuticals Private Limited

Completed

A Bioequivalence Study Using Clinical Endpoint for Diclofenac Sodium Gel 1% in Osteoarthritis Knee"

Osteoarthritis, Knee

India
University of Maryland, Baltimore
Food and Drug Administration (FDA)

Completed

Evaluation of Bioavailability of Diclofenac Dermal Products

Bioavailability

United States
Guy's and St Thomas' NHS Foundation Trust

Active, not recruiting

Urine Alkalinisation to Prevent AKI in COVID-19

Covid19

United Kingdom
Bayero University Kano, Nigeria

Unknown

Intracervical Lidocaine Versus Intramuscular Diclofenac for Pain Relief in HSG in a Tertiary Hospital in Kano

Female Infertility of Tubal Origin

Nigeria
GlaxoSmithKline

Completed

Rosiglitazone Versus a Sulfonylurea On Progression Of Atherosclerosis In Patients With Heart Disease And Type 2 Diabetes

Atherosclerosis

United States, Russian Federation, Spain, Germany, Korea, Republic of, Sweden, Canada, Netherlands, Thailand, Hong Kong, Argentina, France, Mexico, Greece, Poland, Italy, India, Brazil, Latvia, Czech Republic
Imperial College London

Completed

Oral Propionate to Treat and Prevent Diabetes

Diabetes Mellitus

United Kingdom
Cerimon Pharmaceuticals
PPD

Completed

Diclofenac Patch for Treatment of Mild to Moderate Tendonitis or Bursitis

Rotator Cuff Tendonitis | Bicipital Tendonitis | Subdeltoid Bursitis of the Shoulder | Subacromial Bursitis of the Shoulder | Medial Epicondylitis of the Elbow | Lateral Epicondylitis of the Elbow | DeQuervain's Tenosynovitis of the Wrist

United States
Knight Therapeutics (USA) Inc

Withdrawn

Treatment of Leishmaniasis With Impavido® (Miltefosine): Higher-Weight Patient Registry

Leishmaniasis

United States
Cerimon Pharmaceuticals
PPD

Terminated

Diclofenac Patch for Treatment of Mild to Moderate Ankle Sprain

Ankle Sprain

United States
HALEON

Not yet recruiting

A Real-World Evidence Study to Evaluate the Effects of Voltaren Use on Mobility and Quality of Life in Participants With Knee Osteoarthritis Pain

Pain
Fidia Farmaceutici s.p.a.

Completed

Clinical Trial With Diclofenac Sodium Medicated Plaster in Patients With Impact Injuries of the Limbs

Inflammation | Trauma Injury

Hungary, Germany, Italy
Institute of Liver and Biliary Sciences, India

Completed

Sedation for Patients Undergoing Endoscopic Retrograde Cholangiopancreatography

Biliary Colic

India
IBSA Institut Biochimique SA

Completed

Injectable Diclofenac for the Prevention of Post-operative Dental Pain (DP4)

Pain

United Kingdom
Baxalta now part of Shire

Completed

Pharmacokinetic, Safety and Tolerability Study of Recombinant Von Willebrand Factor / Recombinant Factor VIII Complex in Type 3 Von Willebrand Disease

Von Willebrand Disease

United States, Germany, United Kingdom, Italy, Austria, Canada
Hospital Universitario Ramon y Cajal

Completed

Sodium Chloride and Contrast Nephropathy

Heart Failure | Diabetes | Kidney Failure, Chronic | Kidney Failure, Acute

Spain
GlaxoSmithKline

Completed

A Multicenter Efficacy Study of a Diclofenac+Menthol Gel in Subjects With Ankle Sprain

Pain

Germany
Children's Hospital of Orange County
CSL Behring

Completed

Clinical Trial of Factor XIII (FXIII) Concentrate

Hemophilia | Factor XIII Deficiency

United States
Biologische Heilmittel Heel GmbH

Completed

TRAUMED - a Clinical Trial in Acute Ankle Sprain (TRAUMED)

Ankle Sprain

Germany
Stichting Hemato-Oncologie voor Volwassenen Nederland
Astellas Pharma Global Development, Inc.; Deutsch-Österreichische Studiengruppe...

Active, not recruiting

A Study of Gilteritinib Versus Midostaurin in Combination With Induction and Consolidation Therapy Followed by One-year Maintenance in Patients With Newly Diagnosed Acute Myeloid Leukemia or Myelodysplastic Syndromes With Excess Blasts-2 With FLT3 Mutations Eligible for Intensive Chemotherapy (HOVON 156 AML)

Acute Myeloid Leukemia | Myelodysplastic Syndrome With Excess Blasts-2

Netherlands, Belgium, Germany, Switzerland, Australia, Finland, Norway, Sweden, Austria, France, Ireland, Lithuania, Luxembourg, Spain
Sandoz

Completed

To Demonstrate the Relative Bioavailability of Diclofenac Sodium 75 mg Enteric-Coated Tablets Under Non-Fasting Conditions

Inflammation
Grünenthal GmbH
Grünenthal Colombiana S.A.

Completed

Pharmacokinetic Non-interaction Study With a Fixed-dose Combination Tablet With Tramadol and Diclofenac

Pharmacokinetics

Mexico
Sandoz

Completed

To Demonstrate the Relative Bioavailability of Diclofenac Sodium 50 mg Enteric-Coated Tablets Under Non-Fasting Conditions

Inflammation
University of Aarhus

Completed

Lactate in the Gut

Healthy | Hyperlactatemia | Lactate

Denmark
University of Monastir

Completed

Respiratory Variation in Central Venous Oxygen Saturation Predicts Volume Responsiveness in Hemodynamically Unstable Patients Under Mechanical Ventilation : a Prospective Cohort Study (VOS-HI)

Hemodynamic Instability

Tunisia
Boston University

Completed

Phase II Study of Arginine Butyrate With or Without Epoetin Alfa in Patients With Thalassemia Intermedia

Beta-Thalassemia

United States, United Kingdom
Cerimon Pharmaceuticals
PPD

Completed

Diclofenac Patch for Treatment of Acute Pain Due to Mild to Moderate Ankle Sprain (SUPPORT 2)

Acute Pain | Ankle Sprain

United States

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