Search clinical trials for: Heel Cushion Material Bulk (foam)

Total 87 results

Brooke Army Medical Center

Completed

The Influence of Heel Wedge Properties on Roll-over of the Intrepid Dynamic Exoskeletal Orthosis (IDEO)

Physical Disability

United States
Reckitt Benckiser Healthcare (UK) Limited
O4 Research

Completed

A 3 Day In-use Assessment of the Scholl Corn Foam Cushions on Pain Levels Associated With Heloma Durum.

Heloma Durum

Ireland
Prince of Songkla University

Unknown

Heel Cushion for Plantar Fasciitis

Plantar Fasciitis

Thailand
Cairo University

Unknown

Evaluation of Organically Modified Ceramic Resin Composite Versus Bulkfill Resin in Proximal Posterior Cavities

Proximal Caries
Nuh Naci Yazgan University
TC Erciyes University

Completed

Clinical Evaluation of Bulk-fill Composite Resins in Class II Restorations

Dental Composite

Turkey
DeRoyal Industries, Inc.
Lincoln Memorial University

Completed

Evaluation of Heel Offloading Devices for Reducing Heel Contact Pressures in Healthy Volunteers

Heel Pressure Ulceration Prevention Strategies

United States
Ivoclar Vivadent AG
KU Leuven

Active, not recruiting

Trial With Two New Tooth-colored Restorative Materials in Class I/II Cavities

Caries | Defective Restorations

Belgium
University of Pittsburgh
Eunice Kennedy Shriver National Institute of Child Health and Human Development...

Completed

An RCT on Preventing Pressure Ulcers With Wheelchair Seat Cushions

Pressure Ulcer

United States
Hacettepe University

Active, not recruiting

Comparison of Bulk-Fill Composite Resins in Class II Restorations

Class II Dental Caries

Turkey
Maastricht University Medical Center

Completed

Assessment of Bioavailability of Phenolics From an Orange Peel Extract

Improving Bioavailability

Netherlands
Izmir Katip Celebi University

Completed

Nano-Hybrid vs Bulk-Fill Resin Composites

Dental Caries in Children | Composite Resin

Turkey
Vyne Therapeutics Inc.
Premier Research Group plc

Completed

A Study (Study 1) to Evaluate the Safety and Efficacy of FMX103 1.5% Topical Minocycline Foam in the Treatment of Facial Papulopustular Rosacea

Facial Papulopustular Rosacea

United States
Vyne Therapeutics Inc.
Premier Research Group plc

Completed

A Study (Study 2) to Evaluate the Safety and Efficacy of FMX103 1.5% Topical Minocycline Foam in the Treatment of Facial Papulopustular Rosacea

Facial Papulopustular Rosacea

United States
Vyne Therapeutics Inc.

Completed

A Study to Compare the Efficacy and Safety of Topical Administration of FMX-101 for Treatment of Moderate-to-Severe Acne

Acne Vulgaris

United States, Dominican Republic
Vyne Therapeutics Inc.

Completed

A Study to Compare the Efficacy and Safety of Topical Administration of FMX-101 for Treatment of Moderate-to-Severe Acne

Acne Vulgaris

United States, Dominican Republic
Vyne Therapeutics Inc.

Completed

Safety and Efficacy Study of a Topical Minocycline Foam in Patients With Papulopustular Rosacea (EMIRA)

Rosacea | Papulopustular Rosacea

Germany
Vyne Therapeutics Inc.

Completed

Clinical Study to Evaluate Tolerability and Safety of FXFM244 and to Monitor Clinical Effect in Acne Vulgaris Patients

Acne Vulgaris

Israel
Next Science TM
Advancing the Zenith of Healthcare

Terminated

Evaluating Wound Healing With Next Science Gel & Wash.

Chronic Wound

United States
Cairo University

Not yet recruiting

Evaluation of the Proximal Contact Quality in Posterior Complex Carious Cavities Restored With Bulk Fill Ormocer and Resin Composite Using a Precontoured Circumferential Matrix System Versus Pre Contoured Sectional Matrix System

Posterior Complex Carious Proximal Cavities

Egypt
Vyne Therapeutics Inc.

Completed

A Pharmacokinetic Study of Minocycline in Male and Female Volunteers

Acne

Israel
University of Michigan

Completed

The Fruit and Vegetable Study

Cancer

United States
Vyne Therapeutics Inc.

Terminated

Study to Evaluate the Safety and Efficacy of Topical Minocycline FXFM244 in Rosacea Patients

Rosacea

Israel
Vyne Therapeutics Inc.

Completed

Study to Evaluate the Safety and Efficacy of Topical Minocycline FXFM244 in Impetigo Patients

Impetigo

Israel
Exactech

Terminated

Evaluation of Radiographic and Patient Outcomes Following Lumbar Spine Fusion Using Demineralized Bone Matrix (DBM) Mixed With Autograft

Degenerative Disc Disease | Spondylolisthesis | Stenosis

United States
Tristate Brain and Spine Institute

Suspended

Clinical and Radiological Outcomes of Oblique Lateral Lumbar Interbody Fusion

Lumbar Disc Herniation | Degenerative Disc Disease | Spondylolisthesis

United States
Second Affiliated Hospital, School of Medicine,...

Completed

LLIF Plus Posterior Decompression for Severe Lumbar Spinal Stenosis

Lumbar Spinal Stenosis | Lumbar Spine Degeneration

China
Vyne Therapeutics Inc.

Completed

A Study to Compare FCD105 Foam to Minocycline 3% Foam, Adapalene 0.3% Foam and Vehicle Foam.

Acne Vulgaris

United States
Vyne Therapeutics Inc.

Completed

A Study to Evaluate the Efficacy and Safety of Topical Administration of FMX101 in the Treatment of Moderate-to-Severe Acne Vulgaris

Acne Vulgaris

United States
Second Affiliated Hospital, School of Medicine,...
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical... and other collaborators

Unknown

A Modified Lateral Lumbar Interbody Fusion VS. Transforaminal Lumbar Interbody Fusion for Adult Degenerative Scoliosis

Degenerative Scoliosis | Spinal Deformity | Minimally Invasive

China
Medtronic Spinal and Biologics

Terminated

OLIF25™ /OLIF51™ Study

Scoliosis | Degenerative Disc Disease

United States, France, Belgium, Czechia, Italy, Portugal, Puerto Rico
Hospital for Special Surgery, New York

Withdrawn

Indirect vs. Direct Decompression for Treatment of Central Stenosis: RCT (IDVD)

Patients With Spinal Stenosis Indicated for LLIF

United States
Becton, Dickinson and Company

Completed

A 7 Day Adhesive Device Wear Study to Evaluate BD StatLock™ Devices

Peripheral Intravenous Catheter Stabilization

United States
Xuanwu Hospital, Beijing

Recruiting

Impact of Lateral Bone Grafting With Intraoperative Fusion in ACDF on Clinical Outcomes

Cervical Spondylosis

China
University of Southampton
University of Nottingham; Norfolk and Norwich University Hospitals NHS Foundation... and other collaborators

Not yet recruiting

Cellulitis Optimal Antibiotic Treatment (COAT)

Cellulitis of Leg
B. Braun Medical Inc.

Completed

Pharmacokinetics and Safety of Cefazolin 3gm DUPLEX in Adults (3gCefPK)

Infections

United States
Seoul National University Hospital

Recruiting

Comparison of Surgical Outcomes Between Pre Sympathetic Plexus and Post Sympathetic Plexus Approach

Fusion of Spine | Sympathetic Nervous System

Korea, Republic of
Edward Lain, MD
Vyne Therapeutics Inc.

Completed

A Companion Treatment Study for Patients With Moderate to Severe Acne Vulgaris

Acne Vulgaris

United States
Beth Israel Deaconess Medical Center
Biocodex

Completed

Effects of S. Boulardii and Amoxicillin/Clavulanate on Gut Microbiota

Healthy Volunteers

United States
Vyne Therapeutics Inc.

Completed

Safety, Tolerability and Efficacy Study of Doxycycline Foam for the Prevention of EGFRI Skin Toxicity in Cancer Patients

Rash Due to Epidermal Growth Factor Receptor Inhibitors

Israel
Southern Medical University, China

Recruiting

Clinical Study of the Treatment of Chiari Malformation Combined With Type II Skull Base Depression

Chiari Malformation | Basilar Invagination | Atlantoaxial Dislocation

China
Gaffree & Guinle Universitary Hospital
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.; Conselho Nacional...

Recruiting

Protocol for an Analytical Study With Microbiological, Phenotypic, Genotypic and Multiomics Techniques

Degenerative Disc Disease | Back Pain, Low

Brazil
Hamad General Hospital

Recruiting

To Assess Use of Vancomycin Powder in Craniotomy on Wound Infection Rates

Wound Infection

Qatar
Istituto Ortopedico Galeazzi

Completed

Gait Analysis Following Total Ankle Replacement and Subtalar Fusion

Ankle Osteoarthritis

Italy
National University Hospital, Singapore
Merck Sharp & Dohme LLC

Unknown

An Observational Study of Ertapenem in Outpatient Parenteral Antibiotic Therapy (OPAT) for Complicated Urinary Tract Infections.

Urinary Tract Infections

Singapore
CMC Ambroise Paré

Completed

Isthmic Spondylolisthesis Treated With Combined Approach: Clinical and Radiological Outcomes (SPLAC)

Surgical Procedure, Unspecified | Isthmic Spondylolisthesis

France
Wyeth is now a wholly owned subsidiary of Pfizer
PETHEMA (Program for the Study and Treatment of Haematological Malignances)

Completed

Study Comparing Piperacillin-tazobactam Versus Piperacillin-tazobactam Plus Glycopeptide in Neutropenic Patients

Lymphoma | Leukemia | Stem Cell Transplantation | Myelodysplasia | Myeloma | Hematological Malignancy

Spain
Institute of Liver and Biliary Sciences, India

Completed

Comparison of 9 Doses vs 3 Doses of Post Operative Antibiotics in Live Liver Donors

Postoperative Infection | Antibiotic Prophylaxis

India
Gary Goldenberg

Completed

Treatment of Staphylococcus Aureus Colonization in Hand Eczema

Hand Eczema | Foot Eczema

United States
Otic Pharma

Completed

Efficacy and Safety of Once-Daily Ciprodexa Otic Foam Compared to Twice-daily Ciprodex Ear Drops in Acute Otitis Externa (Ciprodexa Foam)

Otorhinolaryngologic Diseases | Ear Diseases | Otitis Externa | Otitis

Israel
Turku University Hospital
Oulu University Hospital; Seinajoki Central Hospital; Tampere University Hospital and other collaborators

Active, not recruiting

Appendicectomy Versus Antibiotics in the Treatment of Acute Uncomplicated Appendicitis (APPAC)

Acute Appendicitis

Finland

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