Clinical Trials Logo

Pressure Ulcer clinical trials

View clinical trials related to Pressure Ulcer.

Filter by:

NCT ID: NCT00763282 Completed - Clinical trials for Spinal Cord Injuries

Self-Management to Prevent Ulcers in Veterans With SCI (Spinal Cord Injury)

Start date: November 2008
Phase: N/A
Study type: Interventional

Pressure ulcers (PrUs) are the most frequent significant medical complication after spinal cord injury (SCI). PrU prevalence, morbidity, mortality, and recurrence rates are high, and most persons with SCI will have at least one serious PrU during their lifetime. VA costs of treating the almost 3,500 unique Veterans with SCI and a severe ulcer at an SCI Center in FY10 was just under $400 million.

NCT ID: NCT00759889 Completed - Diabetic Foot Clinical Trials

Obtaining and Storing Standard of Care Wound Biopsies for Immediate or Future Wound-Related Scientific Study

Start date: March 2007
Phase:
Study type: Observational

The objective of this study protocol is to use wound biopsies that have been obtained during standard of care management for further scientific evaluation after standard evaluation by a pathologist. Further imaging and molecular analyses would closely evaluate the presence, architecture, and interaction of wound biofilm and human host tissues.

NCT ID: NCT00665535 Completed - Pressure Ulcers Clinical Trials

Pressure Ulcer Prevention: Turning for Ulcer Reduction

TURN
Start date: March 2008
Phase: Phase 3
Study type: Interventional

The purpose of the study is to determine the optimal frequency of repositioning nursing facility residents with limited mobility who are cared for on a high density foam mattress in order to prevent bed sores. It is hypothesized that participants at moderate risk (Braden Scale Scores 13-14) who are turned every 3 or 4 hours and participants at high risk (Braden Scores 10-12) turned every 3 or 4 hours will not have a higher incidence of ulcers than those residents turned every 2 hours.

NCT ID: NCT00628602 Completed - Pressure Ulcer Clinical Trials

BION Active Seating for Pressure Ulcer Prevention

Start date: November 2007
Phase: Phase 1
Study type: Interventional

Pressure ulcers (PUs) are a debilitating pathology resulting from pressure and shear in the soft tissues of immobilized patients. In studies to date, BION neuromuscular stimulation has been demonstrated to activate strong muscle contractions and to produce skeletal motion, with associated increases in muscle bulk (hypertrophy), strength, and metabolic capacity, hence counteracting the 3 major etiological factors in PU development (immobility, soft-tissue atrophy and hypoxia). This study intends to use neuromuscular stimulation to both shift paralyzed subjects' weight and build up gluteal muscle volume, in order to prevent recurrence of pressure ulcers. We will implant BIONs alongside the already exposed inferior gluteal and sciatic nerves in patients who are undergoing gluteal rotation flap surgery for PU reconstruction. The gluteal rotation flap is a common reconstructive technique for treating PUs by bringing healthy muscle and skin in to repair the deficient area, and to provide healthy tissue covering over bony prominences. The implanted BIONs will enable us subsequently to stimulate the gluteus maximus and hip extensor muscles. Outcome measures will include tissue health variables (measured by clinical assessment, X-Rays, MRI and Sesta-MIBI SPECT perfusion scans), pressure redistribution (measured by an array of pressure sensors), and recurrence rates over 12 months.

NCT ID: NCT00624806 Completed - Spinal Cord Injury Clinical Trials

Developing a Home Telehealth Program to Manage Pressure Ulcers in SCI/D

Start date: February 2008
Phase: N/A
Study type: Interventional

The Veteran's Health Administration (VHA) is a national leader in using distance technology to monitor patients' self-care via an in-home messaging device with disease management protocols (DMPs). No such DMPs exist for the community dwelling spinal cord injury/disorders (SCI/D) population. Our objective is to develop the tools necessary for implementing a new home telehealth program to manage community-dwelling veterans with SCI/D at high risk of developing pressure ulcers (PrUs).

NCT ID: NCT00521027 Completed - Diabetic Foot Clinical Trials

Study Comparing VERSAJET With Conventional Surgical Procedures in the Removal of Unhealthy Tissue From Lower Limb Ulcers

Start date: April 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the VERSAJETâ„¢ device with conventional surgical procedures (performed with a scalpel) in the debridement (removal of unhealthy tissue) of lower limb ulcers. It is hypothesised that the time taken to debride lower limb ulcers will be quicker with the VERSAJETâ„¢ device than with conventional surgical procedures.

NCT ID: NCT00507650 Completed - Pressure Ulcers Clinical Trials

Increasing Fluids in Older Adults to Prevent & Treat Pressure Ulcers

Start date: September 2003
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether providing extra fluid to nursing home residents will help prevent or heal pressure ulcers. We hypothesize that providing extra fluid to nursing home residents will increase their skin blood flow and oxygen to support healing and maintaining healthy skin. Participants are enrolled who have a pressure ulcer or who are at-risk for an ulcer (determined by looking at risk factors). The study is divided into two 10 day phases. In Phase 1, we examine participant's usual status, including fluid intake and baseline healing potential. In Phase 2, participants are randomly placed in groups to receive either their usually prescribed fluid intake or additional fluid. A study nurse provides the fluid to the residents. We measure their actual intake, their body water, how well their kidneys are working, their potential to heal, and also monitor them for the development of fluid overload. This study is important because it helps us understand the role of a basic nursing intervention in the prevention and treatment of pressure ulcers.

NCT ID: NCT00487097 Completed - Intensive Care Clinical Trials

The Effect of Antioxidants on the Immune Response and Wound Healing in Critically Ill Patients

Start date: September 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate whether the addition of omega-3 and antioxidants to nutritional support in critically ill patients in the intensive care unit influences the immune and anti-inflammatory systems and so improves wound healing.

NCT ID: NCT00405834 Completed - Pressure Ulcers Clinical Trials

A Pilot Study of the Envision® Surface

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

This study is to evaluate the clinical safety and effectiveness of the Envision® surface.

NCT ID: NCT00405795 Completed - Pressure Ulcer Clinical Trials

Envision® Surface Evaluation

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

This observational study will acquire initial clinical practice utilization and product safety data for the Envision® surface.