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Pressure Injury clinical trials

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NCT ID: NCT04761679 Terminated - Pressure Injury Clinical Trials

Nasal Bridge Pressure Injury Prevention

Start date: March 23, 2021
Phase: N/A
Study type: Interventional

The primary goal of this study is to explore whether applying the Mepilex foam on the nasal bridge directly between the skin and the N95 mask will prevent nasal bridge pressure injury among nursing staff, secondary to long-term ( >8+ hours) wear time. The secondary goal is to evaluate if using the Mepilex maintains the seal of the mask.

NCT ID: NCT04328246 Terminated - Pressure Injury Clinical Trials

Pressure injuRy preventiOn by inTermittent EleCtrical sTimulation

PROTECT
Start date: February 26, 2021
Phase: Phase 3
Study type: Interventional

The proposed study assesses the superiority of IES supplementation to the standard of care alone (offloading pressure every two hours) in improving the prevention and treatment of sacral and ischial pressure injuries.

NCT ID: NCT04023981 Terminated - Pressure Ulcer Clinical Trials

Parafricta Bootees vs UK Standard Care to Prevent Heel Pressure Ulcers

Start date: October 26, 2017
Phase: N/A
Study type: Interventional

This randomised study will assess whether Parafricta bootees, when used in addition to normal standard care, can reduce the incidence of heel PUs in patients at very high risk of skin breakdown. The participant group will be hospital inpatients at high risk of PUs (Waterlow score of 20 or more) who are bedbound and do not have existing heel PUs. The participants will be randomised to an intervention arm using Parafricta plus standard care, or a control arm of standard care only. The primary outcome is incidence of heel PUs at day 3. Secondary outcomes are incidence of PUs at day 14, length of stay, severity of PUs, patient acceptability of device, cost-effectiveness.

NCT ID: NCT03924622 Terminated - Pressure Injury Clinical Trials

Pressure Injury Prevention in AE and PFC

Start date: July 20, 2019
Phase: N/A
Study type: Interventional

This study evaluates the effect of a multilayer skin dressing (Mepilex) placed on the sacrum or a fluid filled pad (LiquiCell) on risk factors for pressure injuries under conditions consistent with military long-distance transport or prolonged field care. Participants will be assigned to one of six groups - air transport, air transport on a spinal immobilization surface with or without Mepilex or on a field stretcher with or without LiquiCell.