Search clinical trials for: carboxymethylcellulose sodium

Total 10453 results

Allergan

Completed

Safety and Efficacy Study of New Eye Drop Formulations With Refresh Tears® in Patients With Dry Eye Disease

Dry Eye Syndromes

Canada, Australia
Allergan

Completed

A Study to Compare the Safety and Efficacy of a New Eye Drop Formulation With REFRESH PLUS® in Participants Following LASIK Refractive Surgery

Bilateral LASIK Surgery

Australia, Canada
Allergan

Completed

A Safety and Efficacy Study of a New Eye Drop Formulation in Patients With Dry Eye Disease.

Dry Eye Syndromes

United States, Australia
Allergan

Completed

A Study to Compare a New Eye Drop Formulation With Refresh Contacts®

Contact Lens Lubrication

United States
Medline Industries

Completed

A Comparative Evaluation of a MPS Dressing and a CMC Dressing on Subjects With Lower Extremity Venous Ulcers

Venous Leg Ulcer

United States
Allergan

Completed

Safety and Acceptability of Using a Rewetting Drop With Contact Lens Wear

Ametropia

United States
Milton S. Hershey Medical Center

Withdrawn

Healing of Persistent Epithelial Defects

Cornea

United States
University College Dublin

Recruiting

Gel for Early Hypoglycaemia Prevention in Preterm Infants (GEHPPI)

Hypoglycemia in Newborn Infants

Czechia, Ireland
Chulalongkorn University

Completed

Comparative Study of 0.5% Carboxymethylcellulose With 0.005% Stabilized Oxychlorocomplex (PURITE™) Versus 0.5% Carboxymethylcellulose in the Treatment of Dry Eye

Dry Eye Syndromes

Thailand
Massachusetts General Hospital
Gelesis, Inc.

Completed

The Effect of CSP01 on Chronic Idiopathic Constipation and Irritable Bowel Syndrome With Constipation

Constipation | Irritable Bowel Syndrome With Constipation | Chronic Idiopathic Constipation

United States
SIFI SpA

Completed

Efficacy of Topical 0.2% Xanthan Gum in Patients With Dry Eye

Dry Eye

Italy
University of Pennsylvania
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK); Georgia...

Completed

Functional Research of Emulsifiers in Humans (FRESH)

Healthy

United States
Rush University Medical Center

Recruiting

Aquacel Hypersensitivity Dressing in TJAs

Contact Allergic Dermatitis | Adverse Skin Reaction

United States
University of Campinas, Brazil
Merck Sharp & Dohme LLC

Completed

The Effects of BAK on the Blood Aqueous Barrier of Pseudophakic Patients

Dry Eye Syndromes

Brazil
Allergan

Completed

A Multi-Center Randomized Study to Evaluate the Efficacy and Safety of an Investigational Lubricant Eye Drop

Dry Eye

United States
ULURU Inc.

Terminated

Altrazeal Range of Motion Study Comparing With Typical Carboxymethyl (ROM)

Burn

United States
Alcon Research

Completed

Kynex Versus Refresh Plus Study in Subject With Dry Eye

Dry Eye
Optometric Technology Group Ltd
Allergan

Completed

Evaluation of the Effect of Repeated Usage on the Tear Film Characteristics of an Investigational Eye Drop in Dry Eye Sufferers

Dry Eye Syndrome

United Kingdom
University of Minnesota

Completed

Dietary Fiber for Fecal Incontinence

Fecal Incontinence

United States
University of Florida

Withdrawn

Oral Glucose Intervention for Children With Gastroenteritis and Ketosis

Ketosis | Gastrointestinal Infections
Rothman Institute Orthopaedics

Unknown

A Prospective, Randomized, Comparative Study to Assess the Prevention of Surgical Site Infection (SSI's) in Revision Total Joint Arthroplasty Patients Treated With Single-Use Negative Pressure Wound Therapy (PICO) or Standard Care Dressings (AQUACEL Ag SURGICAL Dressing).

Surgical Incision

United States
Laboratoires URGO

Unknown

Assessment of Efficacy & Safety for a New Wound Dressing Urgo 310 3166 in the Local Treatment of VLU or Mixed Leg Ulcers

Leg Ulcers

France
Allergan

Completed

A Study to Compare the Safety and Efficacy of A New Eye Drop Formulation With OPTIVE™ in Subjects With Dry Eye Disease

Dry Eye Disease

France, Spain, Russian Federation, Belgium, Germany, Italy, United Kingdom, Australia
Allergan

Completed

Safety and Efficacy of an Artificial Tear for the Treatment of Dry Eye

Dry Eye Syndrome

United States
University of California, Irvine

Terminated

A Randomized Comparison Study of Aquacel Ag and Glucan II as Donor Site Dressings

Burns

United States
Dr Angela Oates
ConvaTec Inc.

Completed

The Effect of Aquacel® Ag+ Extra Dressing on Wound Biofilms

Diabetes | Chronic Foot Wounds

United Kingdom
ULURU Inc.

Completed

Altrazeal™ Versus Aquacel® Ag for Partial Thickness Skin Donor Sites

Partial-thickness Skin Donor Sites

United States
Winthrop University Hospital
Stony Brook University; Lehigh Valley Hospital

Completed

Seprafilm® Adhesion Barrier and Cesarean Delivery

Cesarean Section | Adhesions | Delivery, Obstetric

United States
University of Malaga
BSN Medical GmbH; Andalusian Health Service

Unknown

Effectiveness of a Hydrophobic Dressing for Microorganisms' Colonization and Infection Control of Vascular Ulcers (CUCO-UV)

Bacterial Infections | Venous Leg Ulcer | Chronic Ulcer of Skin of Lower Limb Nos

Spain
Allergan

Completed

Safety and Tolerability of Artificial Tears in Dry Eye Subjects

Dry Eye Syndrome

United States
Bucheon St. Mary's Hospital

Completed

The Effect of Guardix-solution for the Prevention of Postoperative Intestinal Adhesion and Intestinal Obstruction After Laparoscopic Pelvic Cavity Surgery

Prostate Cancer | Postoperative Adhesion
Kansas City Heart Rhythm Institute

Completed

Comparison of Outcomes Between the Use of Silverlon® Dressing and AQUACEL® AG Dressing Post Cardiac Device Implant

Wounds and Injuries | Infections

United States
ConvaTec Inc.

Completed

A Single Centre, Randomised, Comparative, Blinded Wear Test of Two Adhesives on the AQUACEL® Foam Adhesive Dressing

Safety and Performance of Dressing Adhesive on Healthy Volunteers

United Kingdom
Molnlycke Health Care AB

Completed

Evaluation of Exufiber Ag+ and Other Gelling Fibre Dressings

Wounds and Injuries

United States
Allergan

Completed

Safety and Efficacy of Two Artificial Tears in Dry Eye Subjects

Dry Eye Syndrome

United States
UPM Biomedicals
Helsinki University Central Hospital

Not yet recruiting

Post-market Clinical Follow-up Study for a CE Marked Wound Care Product (FibDex®)

Skin Transplantation
University Hospital, Ghent

Completed

Bacterial Control in Partial Thickness Burns Using Silver-containing Wound Dressings

Burn Wounds - Partial Thickness (2nd Degree)

Belgium
ConvaTec Inc.

Completed

Study to Evaluate the Performance of AQUACEL® Extra™ in Venous Leg Ulcers

Leg Ulcer

United Kingdom, Germany, Netherlands, Poland
Allergan

Completed

Evaluate the Safety and Efficacy of a New Artificial Tear for Use After LASIK Surgery

Dry Eye Syndrome

United States
Allergan

Completed

Study to Compare the Efficacy and Safety of Two Non-Preserved Artificial Tears for the Treatment of Dry Eye Signs and Symptoms

Dry Eye Syndromes

Germany
Allergan

Completed

Safety, Efficacy, and Acceptability Study of an Eye Drop Formulation in Subjects With Dry Eye Disease

Dry Eye Syndromes

United States
Golden Jubilee National Hospital
ConvaTec Inc.

Withdrawn

Study of AQUACEL™ Ag Surgical Cover Dressing Following Total Knee Replacement

Osteoarthritis
ConvaTec Inc.

Completed

Compare Aquacel® Ag Versus Mepilex® Border Ag to Manage Bioburden in Leg Ulcers

Leg Ulcers

United Kingdom
Allergan

Completed

A Safety and Efficacy Study of Refresh Optive® Gel Drops in Patients With Dry Eye Disease

Dry Eye Syndromes

United States
ConvaTec Inc.

Completed

AQUACEL® Ag Dressing and Urgotul® Silver Dressing on Healing of Chronic Venous Leg Ulcers

Leg Ulcer

Denmark, France, Germany, Poland, United Kingdom
Allergan

Completed

Performance and Acceptance of Optive Versus Hylocomod Eyedrops in Patients With Dry Eye Symptoms

Dry Eye Syndromes

United Kingdom
Allergan

Completed

A Study to Compare a New Eye Drop Formulation With Systane® Gel Drops and Genteal® Lubricant Gel Drops for Moderate to Severe Dry Eye Relief

Dry Eye Syndromes

United States
University of Florida

Completed

Effects of Carboxymethylcellulose Artificial Tears on the Eye Microbiome

Dry Eye Syndromes

United States
Moses Murandu
University of Birmingham; Laboratoires URGO; University of Wolverhampton

Unknown

Use of White Granulated Sugar on Wounds

Infected Wounds

United Kingdom
ConvaTec Inc.
NAMSA

Completed

AQUACEL® Ag+ Extra™ and Cutimed™ Sorbact® Dressing in the Management of Venous Leg Ulcers Over a 12-week Period

Diabetic Foot | Venous Leg Ulcer

Germany, Colombia, United Kingdom

3

Subscribe