Search clinical trials for: 0.9% sodium chloride (normal saline)

Total 6387 results

Mukoviszidose Institut gGmbH
Cystic Fibrosis Foundation

Completed

Efficacy and Safety Study of Inhaled Glutathione in Cystic Fibrosis Patients

Cystic Fibrosis

Germany
Virginia Commonwealth University

Withdrawn

Ideal Initial Bolus and Infusion Rate for Erector Spinae Plane Block Catheters

Pain, Postoperative | Pain, Chest

United States
University of Edinburgh
Kidney Cancer UK

Terminated

Heme Arginate in Transplantation Study (HOT2)

Renal Transplant Rejection | Renal Transplant Failure

United Kingdom
Seoul St. Mary's Hospital
Green Cross Corporation

Terminated

The Efficacy and Safety Study of ALbumin Therapy in Acute Ischemic Stroke (ALbumin)

Cerebral Infarction

Korea, Republic of
University of Alabama at Birmingham

Withdrawn

Superficial Cervical Plexus Blockade for Clavicle Fracture Analgesia

Pain, Postoperative | Satisfaction

United States
The First Affiliated Hospital of Nanchang University

Completed

Fecal Microbiota Transplantation for Pancreatitis (FMTP)

Acute Pancreatitis | Intestinal Bacteria Flora Disturbance | Fecal Microbiota Transplantation | Intestinal Dysfunction

China
BioAegis Therapeutics Inc.

Completed

A Phase 1b/2a Study of the Safety and Pharmacokinetics of Rhu-plasma Gelsolin in Hospitalized Subjects With CAP

Community-acquired Pneumonia

Australia, Georgia
University of California, San Diego

Completed

An Analysis of the Effect of Topical Cromolyn Sodium on Rosacea-associated Erythema

Papulopustular Rosacea

United States
Invivyd, Inc.
Novotech (Australia) Pty Limited

Active, not recruiting

A Study to Investigate the Safety, Tolerability, and Pharmacokinetics of the Monoclonal Antibody VYD222 in Healthy Adult Participants

COVID-19

Australia
MassBiologics
Celerion

Completed

First Clinical Study of the Safety and Blood Levels of a Human Monoclonal Antibody (2217LS) Against Lyme Disease Bacteria in Healthy People

Lyme Disease

United States
Guangdong Women and Children Hospital

Unknown

The Treatment of Premature Infants With Brain Injury by Autologous Umbilical Cord Blood Stem Cells

Safety Issues | Effect of Drugs
Federal University of Mato Grosso

Completed

Body Composition and Serum Biochemistry After Intravenous Infusion or Oral Intake of Saline in Healthy Volunteers

Edema | Perioperative/Postoperative Complications

Brazil
MiMedx Group, Inc.

Completed

Micronized dHACM Injectable for the Treatment of Plantar Fasciitis (dHACM)

Fasciitis, Plantar

United States
Green Cross Wellbeing
Chung-Ang University Hosptial, Chung-Ang University College of Medicine

Recruiting

Investigator Initiated Trial to Evaluate Efficacy and Safety of LAENNEC (Human Placenta Hydrolysate) Administered by Ultrasonography Guided Subacromial Bursa Injection in Patients With Shoulder Impingement Syndrome (PAIN)

Shoulder Impingement Syndrome

Korea, Republic of
Arrowhead Pharmaceuticals

Completed

Study of ARO-ANG3 in Healthy Volunteers and in Dyslipidemic Patients

Dyslipidemias | Hypertriglyceridemia | Familial Hypercholesterolemia

Australia, New Zealand
Arrowhead Pharmaceuticals

Completed

Study of ARO-APOC3 in Healthy Volunteers, Hypertriglyceridemic Patients and Patients With Familial Chylomicronemia Syndrome (FCS)

Hypertriglyceridemia | Familial Chylomicronemia

Australia, Canada, New Zealand
Alnylam Pharmaceuticals

Completed

A Phase 1/2 Study of an Investigational Drug, ALN-CC5, in Healthy Adult Volunteers and Patients With PNH

Paroxysmal Nocturnal Hemoglobinuria (PNH)

Spain, United Kingdom
Mayo Clinic

Withdrawn

Subcu Administration of CD-NP in Heart Failure Patients With Left Ventricular Assist Device Support (CD-NP/LVAD)

Heart Failure | Left Ventricular Assist Device | Natriuretic Peptide
Australian and New Zealand Intensive Care Research...
Monash University; University College Dublin; Health Research Board, Ireland; Health... and other collaborators

Recruiting

ErythroPOietin Alfa to Prevent Mortality and Reduce Severe Disability in Critically Ill TRAUMA Patients (EPO-TRAUMA)

Wounds and Injuries | Trauma | Traumatic Brain Injury | Multiple Trauma | Major Trauma | Traumatic Injury | Penetrating Injury | Blunt Injury

Australia, Ireland, Finland, New Zealand, Slovenia, Germany, Saudi Arabia, Switzerland
The Catholic University of Korea

Unknown

Effect of Postoperative Ferric Carboxymaltose

Knee Osteoarthritis | Total Knee Arthroplasty | Postoperative Anemia
The Catholic University of Korea

Unknown

Effect of Preoperative Ferric Carboxymaltose After Simultaneous Bilateral Total Knee Arthroplasty

Knee Osteoarthritis | Total Knee Arthroplasty | Postoperative Anemia
BioAegis Therapeutics Inc.

Not yet recruiting

Rhu-pGSN for Acute Respiratory Distress Syndrome (ARDS)

Infections | Acute Respiratory Distress Syndrome
Oxford Brookes University

Completed

Specificity of Dyspnoea Relief With Inhaled Furosemide (FurosAH)

Dyspnea

United Kingdom
National Cancer Institute (NCI)

Active, not recruiting

Vaccine Therapy in Treating Patients With Newly Diagnosed Advanced Colon Polyps

Colorectal Adenoma | Colorectal Adenoma With Severe Dysplasia | Colorectal Tubulovillous Adenoma

United States, Puerto Rico
University of North Carolina, Chapel Hill
National Institute of Allergy and Infectious Diseases (NIAID)

Recruiting

Safety and Immunogenicity of HIV-1 Vaccines C62-M4 or C1C62-M3m4 in Persons With HIV-1 Suppressed on ART (CM HIV-Core008)

HIV-1-infection | HIV Vaccine

United States
University of North Carolina, Chapel Hill
National Institute of Allergy and Infectious Diseases (NIAID)

Completed

Study to Assess Safety and Ability to Induce Immune Responses of HIV-1 Vaccines M3 and M4 Given Alone or in Combination in HIV-infected Adults (M&M)

HIV-1 Infection

United States
McMaster University
GlaxoSmithKline; University of Manchester

Recruiting

Mepolizumab for the Treatment of Chronic Cough With Eosinophilic Airways Diseases (MUCOSA)

Asthma | Eosinophilic Bronchitis | Chronic Cough

Canada
Resolve Therapeutics

Active, not recruiting

Phase 2 Study of RSLV-132 in Subjects With Long COVID

Post-acute Corona Virus 19 (COVID-19) (Long COVID)

United States
MassBiologics

Completed

Evaluate the Safety Pharmacokinetics of a Human Monoclonal Antibody S315 Against Diphtheria Toxin in Healthy Subjects (S315)

Diphtheria

United States
Thomas Jefferson University
Department of Health and Human Services

Completed

Zoledronic Acid in Acute Spinal Cord Injury

Spinal Cord Injury

United States
Alnylam Pharmaceuticals

Completed

A Safety and Tolerability Study of an Investigational Drug, ALN-TTRSC02, in Healthy Subjects

Transthyretin-mediated Amyloidosis (ATTR Amyloidosis)

United Kingdom
Alnylam Pharmaceuticals
The Medicines Company

Completed

A Phase 1 Study of an Investigational Drug, ALN-PCSSC, in Subjects With Elevated Low Density Lipoprotein Cholesterol (LDL-C)

Hypercholesterolemia

United Kingdom
Alnylam Pharmaceuticals

Completed

Trial to Evaluate Safety, Tolerability, and Parmacokinetics of ALN-TTR02 in Healthy Volunteer Subjects

TTR-mediated Amyloidosis

United Kingdom
Alnylam Pharmaceuticals

Completed

Trial to Evaluate Safety and Tolerability of ALN-PCS02 in Subjects With Elevated LDL-Cholesterol (LDL-C)

Elevated LDL-Cholesterol (LDL-C)

United Kingdom
Alnylam Pharmaceuticals

Completed

Trial to Evaluate Safety and Tolerability of ALN-TTR01 in Transthyretin (TTR) Amyloidosis

Transthyretin Mediated Amyloidosis (ATTR)

United Kingdom, France, Portugal, Sweden
University of Tennessee

Completed

Para-cervical Block Prior to Laparoscopic Hysterectomy as an Adjuvant Treatment to Reduce Postoperative Pain.

Pain, Postoperative

United States
Jon Simmons
University of South Alabama

Recruiting

Phase 2 Trial Using rhDNase to Reduce Mortality in COVID-19 Patients With Respiratory Failure (DAMPENCOVID)

Covid19

United States
Menoufia University

Completed

Small Volume Fluid Challenge as a Predictor of Fluid Responsiveness in Patients With Circulatory Failure

Circulatory Failure

Egypt
Beth Israel Deaconess Medical Center

Completed

Effect of Sclerotherapy on Fistulas and Sinus Tracts in Hidradenitis Suppurativa

Hidradenitis Suppurativa

United States
Cumberland Pharmaceuticals

Completed

Efficacy, Safety, and Pharmacokinetics of Intravenous Ibuprofen in Adult Febrile Patients

Fever

Australia, United States, Thailand
Stem Cell Therapeutics Corp.

Terminated

REGENESIS (CA): A Study of NTx™-265: Human Chorionic Gonadotropin (hCG) and Epoetin Alfa (EPO) in Acute Ischemic Stroke Patients (REGENESIS)

Stroke

Canada, India
The Hospital for Sick Children

Completed

0.9% NaCl/Dextrose 5% vs 0.45% NaCl/Dextrose 5% as Maintenance Intravenous Fluids in Hospitalized Children

Hyponatremia

Canada
All India Institute of Medical Sciences, New Delhi
Postgraduate Institute of Medical Education and Research; Jawaharlal Institute... and other collaborators

Completed

Balanced Crystalloid vs. Saline in Children With Septic Shock

Shock | Septic Shock

India
Association Athletes For Transparency
Partnership for Clean Competition; University of Milan School of Medicine; Centre... and other collaborators

Unknown

Evaluation of Erythroferrone as a New Biomarker of Erythropoesis Stimulating Agents (ERYTHROFER-01)

Sports Drug Abuse
Frank Mose
Herning Hospital

Completed

The Effect of Orally Administrated Nitrate on Renal Parameters and Systemic Haemodynamics (APNI)

Hypertension

Denmark
Alnylam Pharmaceuticals

Active, not recruiting

HELIOS-B: A Study to Evaluate Vutrisiran in Patients With Transthyretin Amyloidosis With Cardiomyopathy

Transthyretin Amyloidosis (ATTR) With Cardiomyopathy

United States, Poland, Argentina, Australia, Belgium, France, Germany, Japan, Netherlands, Portugal, Spain, Sweden, United Kingdom, Canada, Czechia, Denmark, Hungary, Ireland, Norway, Korea, Republic of, Austria, Croatia, Israel, Latvia, Lithuan... and more
Universitas Bali Internasional

Completed

The Effects of Intra-articular Platelet-Rich Plasma Injection on The Severity of Knee Osteoarthritis

Osteoarthritis, Knee

Indonesia
Arrowhead Pharmaceuticals

Completed

Study of ARO-HSD in Healthy Volunteers and Patients With Non-Alcoholic Steatohepatitis (NASH) or Suspected NASH

Non-alcoholic Steatohepatitis

New Zealand
Dicerna Pharmaceuticals, Inc.

Completed

Study to Evaluate Safety, Tolerability, PK and PD of DCR-PHXC in PH Type 3 Patients (PHYOX4)

Primary Hyperoxaluria Type 3

United States, Germany, Netherlands, United Kingdom
Arrowhead Pharmaceuticals

Completed

Study of ARO-HBV in Normal Adult Volunteers and Patients With Hepatitis B Virus (HBV)

Hepatitis B

Australia, Hong Kong, New Zealand

Search clinical trials for: 0.9% sodium chloride (normal saline)

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