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Wounds clinical trials

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NCT ID: NCT02146612 Completed - Wounds Clinical Trials

Amino Acid Usage Patterns in Daily Practice

Start date: December 2012
Phase: N/A
Study type: Observational

The present study aims to evaluate the patient profile including medical conditions who use a nutritional supplement along with a balanced and varied diet in Turkey.

NCT ID: NCT02008487 Completed - Pressure Ulcer Clinical Trials

Wound Powder for Pressure Ulcers at End-of-life

RGN107
Start date: April 2013
Phase: N/A
Study type: Interventional

This study will test a special powder for ulcers caused by a variety of conditions such as pressure that sometimes happen when a person is at the end of life. The powder will be applied to these ulcers to see if it helps with pain, odor and drainage (leakage). People who are being cared for by hospice or palliative care organizations will be invited to be in the study. The study will also find out if the powder is easy to use by caregivers as well as improving the comfort and quality of life of the person who has the ulcer.

NCT ID: NCT01973361 Completed - WOUNDS Clinical Trials

Efficacy Study of Ultrasound-Assisted Debridement to Influence Wound Healing

UltraHeal
Start date: December 2013
Phase: N/A
Study type: Interventional

The UltraHeal Study is a randomized controlled trial to compare healing response of low frequency contact ultrasonic-assisted debridement in addition to best practice wound care to best practice wound care alone in a Vascular Surgery Clinic patient population with wounds of the lower extremity.

NCT ID: NCT01921725 Completed - Wounds Clinical Trials

The Clinical Application and Efficacy Verification of an Innovative Carbon Fiber Dressing

Start date: May 2013
Phase: N/A
Study type: Interventional

The research uses hydrophilic-based dressing (KoCarbonTM) which is developed by Medical Technology Company Limited (Bio-medical Carbon Technology; BCT) to investigate the wound healing effects of activated-carbon-fiber-based wound dressing on different types of wounds.The dressing is composed by three layers. The first layer is a material of polyethylene terephthalate (PET) weave which is great breathable; Second layer, the activated carbon fiber cloth, is as the absorption of excess tissue fluid, bacteria and contaminations. It reduces the smell of wound and restrains the development of bacteria. In addition, activated carbon has features of far-infrared and anion, which promote blood circulation, speed up metabolism and shorten the time of wound healing. The third layer is a polyethlene (PE) film, which touches the wound surface and provides the anti-adhesion effects. The aim of this study is to investigate how the application of the dressing affects the wound healing conditions on four different types of wounds, including general traumatic wounds, elective surgery wound, diabetes foot ulcer (level 2) and chronic wounds. Due to the characteristics of great fluid absorption and far-infrared features, the hydrophilic-based dressing (KoCarbonTM) is expected to work perfectly on improving the wound repair conditions.

NCT ID: NCT01864967 Completed - Wounds Clinical Trials

Carbon Dioxide Infusion:Clinical and Histological Appraisal in Chronic Wounds

Start date: March 2007
Phase: N/A
Study type: Observational

Carbon dioxide infusion is a non surgical procedure applied via percutaneous, transdermal and subcutaneous. Increase in the concentration of carbon dioxide decreases pH activating local nitric oxide that stimulates collateral vessels formation, vascular endothelial growth factor and basic fibroblast growth factor. Carbon dioxide infusion restores the blood flow in chronic wounds of the lower limbs.

NCT ID: NCT01824381 Completed - Wounds Clinical Trials

Use of the Amniotic Membrane in Large Wound Epithelialization

MA/GH
Start date: July 2012
Phase: Phase 1
Study type: Interventional

The purpose of this study is to analyze the security application of the amniotic membrane in extensive wounds in the granulation phase.

NCT ID: NCT01813305 Completed - Diabetes Mellitus Clinical Trials

CSTC1 for Diabetic Foot Ulcers Phase II Study

Start date: July 9, 2014
Phase: Phase 2
Study type: Interventional

The objective of this study is to evaluate the efficacy and safety of CSTC1 in patient with diabetic foot ulcers.

NCT ID: NCT01807650 Completed - Wounds Clinical Trials

Oleogel-S10 in Wound Healing of Split-Thickness Skin Graft Donor Sites (BSG-12)

BSG-12
Start date: March 2013
Phase: Phase 3
Study type: Interventional

The main purpose of this phase III clinical trial was to show safety and efficacy of Oleogel-S10 in accelerating the wound healing of Split-Thickness Skin Graft (STSG) donor sites.

NCT ID: NCT01683344 Recruiting - Wounds Clinical Trials

Clinical and Health Economic Study of PICO in a Community Care Setting

Start date: January 2012
Phase: Phase 4
Study type: Interventional

The current study is being conducted to assess the clinical and cost effectiveness of managing patients with a chronic or sub-acute wound in a community setting with PICO and to explore the patient experience and issues of concordance that affect patients treated with PICO.

NCT ID: NCT01657305 Completed - Wounds Clinical Trials

Oleogel-S10 in Wound Healing of Split-Thickness Skin Graft Donor Sites (BSH-12)

Start date: August 2012
Phase: Phase 3
Study type: Interventional

The main purpose of this phase III clinical trial was to compare intra-individually the efficacy, safety and tolerability of Oleogel-S10 and non-adhesive wound dressing versus non-adhesive wound dressing only in accelerating the wound healing of Split-Thickness Skin Graft (STSG) donor sites.