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Pressure Ulcer clinical trials

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NCT ID: NCT03125421 Completed - Pressure Sores Clinical Trials

Prevention of Pressure Sores in the Prone Position in ARDS Patients

PSA
Start date: April 16, 2018
Phase: N/A
Study type: Interventional

A nursing strategy to prevent pressure sores in the prone position in Acute Respiratory Distress Syndrome (ARDS) patients. A multicenter controlled prospective stepped wedge trial.

NCT ID: NCT03121144 Completed - Pressure Ulcer Clinical Trials

Usability Validation of Patient Monitoring Device for Pressure Injury Prevention and Fall Detection

Start date: March 1, 2017
Phase: N/A
Study type: Interventional

This study describes a procedure to collect a subject's position, movement, physiological data and usability information using Masimo's investigational device.

NCT ID: NCT03114800 Completed - Pressure Ulcer Clinical Trials

Monitoring Movement for Pressure Ulcer Prevention

Start date: August 9, 2017
Phase: N/A
Study type: Interventional

The goal of this work is to develop and test an automated movement detection monitoring tool that could lead to reduced burden on clinicians and in-turn reduce pressure ulcer incidence rates. Ten healthy participants will perform video-recorded bed movements while weight distribution and interface pressures at bony prominences on the pelvis are recorded.

NCT ID: NCT03070938 Completed - Pressure Ulcer Clinical Trials

PuraPly™ Antimicrobial Wound Matrix and Wound Management

PuraPlyAM
Start date: November 2016
Phase: N/A
Study type: Observational

The PuraPly Antimicrobial Wound Matrix (PuraPly AM) case series is a prospective, observational study for patients who have received PuraPly AM which consists of a collagen sheet coated with polyhexamethylenbiguanide hydrochloride (PHMB) and is intended for the management of wounds; no experimental intervention is involved.

NCT ID: NCT03070925 Completed - Pressure Ulcers Clinical Trials

Prospective PuraPly™ AM Case Series Study

Start date: November 2016
Phase: N/A
Study type: Observational

The PuraPly AM case series is a prospective, observational study for patients who have received PuraPly AM which consists of a collagen sheet coated with polyhexamethylene biguanide hydrochloride (PHMB) and is intended for the management of wounds; no experimental intervention is involved.

NCT ID: NCT03039179 Completed - Pressure Ulcer Clinical Trials

Polyurethane Foam on the Heel for Prevention in Children

SCHIUMABIMB
Start date: July 1, 2014
Phase: N/A
Study type: Interventional

The post-operative treatment of pediatric patients operated for the correction of flat foot, sees today the use of preformed leg-foot splint (Walker) as an alternative to the application of plaster casts. The change of the immobilization system has led to the appearance of problems of tolerability in particular in the skin. The aim of the study is to assess whether by placing a polyurethane foam dress at the heel in the immediate postoperative period until removal of the Walker, the rate of skin lesion and pain is reduced.

NCT ID: NCT03039153 Completed - Knee Osteoarthritis Clinical Trials

Pressure Ulcers in Knee Replacement Surgery

peripress
Start date: March 21, 2017
Phase:
Study type: Observational

From the point of view of nursing to know exactly the different risk factors for the onset of pressure ulcers is very important as it allows to accurately orient preventive care interventions. All the variable that could influence the development of pressure ulcer in patients undergoing knee replacement surgery are identified and collected: age, sex, body max index, risk to develop Pressure Ulcer (braden score), treatment to prevent pressure ulcers (typology of the devices used, such as air mattresses with alternating or static pressure, heel drains, frequency of mobilization carried out by both the patient care), management of eventual incontinence (use of diapers, urinary catheter), type of anesthesia, type of analgesia, length of stay, the ASA physical status classification system (ASA score), comorbidity, cancer, use of devices for controlling the position of the operated limb (foam valve), the number of physical therapy sessions actually carried out.

NCT ID: NCT03021811 Completed - Diabetic Foot Ulcer Clinical Trials

EUREKA Italy - Evaluation of Real-life Use of KLOX BioPhotonic System in Chronic Wounds Management

Start date: October 2015
Phase: N/A
Study type: Interventional

Multi-center, prospective, interventional, uncontrolled open-label study evaluating the real-life use of KLOX LumiHeal BioPhotonic System in chronic wounds management (venous leg ulcers, diabetic foot ulcers, pressure ulcers).

NCT ID: NCT03010293 Completed - Clinical trials for Bone Diseases, Infectious

Pressure Ulcer-associated Osteomyelitis: Evaluation of a Two-stage Surgical Strategy With Prolonged Antimicrobial Therapy

Start date: June 2016
Phase: N/A
Study type: Observational

Pressure ulcer represents a frequent clinical condition in patient with spinal cord injury or after prolonged Intensive Care Unit (ICU) stay. Osteomyelitis constitutes a severe complication with a poorly known management, and is associated with a high rate of relapse, leading to a high-burden in hospital bed-days, financial cost, surgical intervention, antibiotic use, morbidity and mortality, and nursing care. In our reference center for bone and joint infection management, the medical and surgical strategies are systematically discussed during pluridisciplinary meetings. Most patients benefit from a two-stage surgical strategy (debridement with initiation of vacuum-assisted closure therapy until reconstruction using muscular flap) with prolonged antimicrobial therapy. In this context, our study aims to evaluate this complex approach and to determine risk factors of treatment failure in order to improve patient management, focusing on optimization of empirical antimicrobial therapy after each surgical stage, delay between the two surgical stage, and duration of antimicrobial therapy.

NCT ID: NCT02996331 Completed - Pressure Ulcer Clinical Trials

Preventing Pressure Ulcers With Repositioning Frequency and Precipitating Factors

Start date: May 16, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether repositioning frequency can be extended for nursing home (NH) residents who are low, moderate, and high risk for pressure ulcer (PrU) development. The investigators will also determine how changes in medical severity interact with changes in risk level and repositioning schedule to predict PrU development. This study will advance knowledge about repositioning frequency and clinically assessed PrU risk-level in relation to medical severity. Outcomes of this research will contribute to future guidelines for more precise preventive nursing practices and refinement of PrU prevention guidelines.