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58 studies found for:    Open Studies | "Pressure Ulcer"
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Study Details
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Dates
Rank Status Study
1 Recruiting Leptospermum Scoparium Honey and Wound Care for Pressure Ulcers
Condition: Pressure Ulcers
Interventions: Other: Leptospermum scoparium honey;   Other: Standard of Care Treatment
2 Not yet recruiting Clinical Trial of ECLIPSE PRP™ Wound Biomatrix in Chronic Non-Healing Pressure Ulcers
Condition: Pressure Ulcer
Interventions: Device: Eclipse PRP™ Wound Biomatrix;   Other: Usual and Customary Practice
3 Recruiting Low-level Laser Therapy Versus High Frequency on Pressure Ulcers Treatment
Condition: Pressure Ulcer
Interventions: Device: Low-level laser therapy AlGaInP;   Device: High-frequency therapy with O3 formation;   Other: Wound dressing with saline solution
4 Not yet recruiting The Effectiveness of a Pressure Ulcer Prevention Programme for Older People in For-profit Private Nursing Homes
Condition: Pressure Ulcer
Interventions: Behavioral: PU prevention programme;   Behavioral: Usual PU prevention care
5 Recruiting Trial Comparing SOC +Skin IQ MCM vs SOC for Pressure Ulcer (PU)
Condition: Pressure Ulcer
Interventions: Device: Skin IQ™ MCM Coverlet;   Other: Pressure redistribution surface
6 Recruiting Preliminary Study Leading to Prevention of Pressure Ulcers by the Use of an On-board Device : Ergonomic Assessment of Wheelchair-seat Pressures in Spinal Cord Injured (SCI) Patients ( PRESDIE)
Condition: - Pressure Ulcers
Intervention: Device: TexiMat
7 Recruiting Study of SANTYL® vs Hydrogel (SoloSite®) for Pressure Ulcers
Condition: Pressure Ulcer
Interventions: Biological: Santyl;   Biological: SoloSite®
8 Recruiting Pressure Sensing to Reduce the Risk of Pressure Ulcer Formation
Condition: Pressure Ulcer
Intervention: Device: ForeSite PT™ system
9 Not yet recruiting Pressure Ulcer Monitoring Platform (PUMP)
Condition: Pressure Ulcer
Intervention: Behavioral: PUMP Monitoring
10 Recruiting Wound Management for Sacral Pressure Ulcers With Necrotic Tissue
Condition: Pressure Ulcers
Interventions: Device: TheraHoney HD;   Device: SkinTegrity
11 Recruiting Effectiveness of Aurix Therapy in Pressure Ulcers
Condition: Pressure Ulcer
Intervention: Device: Aurix
12 Recruiting Efficacy and Safety of MedifoamⓇ and BetafoamⓇ in Pressure Ulcer
Condition: Pressure Ulcer
Interventions: Device: Foam Dressing;   Device: Foam Dressing with Povidone Iodine
13 Not yet recruiting Pressure Redistributing Overlay With Targeted Cooling Technology (PRO-TECT) for Pressure Ulcer Prevention
Condition: Pressure Ulcer
Intervention: Device: PRO-TECT
14 Recruiting Evaluation of the SEM Scanner 200 for the Detection of Early Pressure Ulcers: A Multi-Site Longitudinal Study
Condition: Pressure Ulcers
Interventions: Device: Use of SEM200 Scanner daily;   Other: Assessment and treatment of Pressure Ulcers using SOC
15 Recruiting Effectiveness of Two Silicone Dressings for Sacral and Heel Pressure Ulcer Prevention
Condition: Pressure Ulcer
Intervention: Device: Mepilex® Border Sacrum and Mepilex® Border Heel
16 Recruiting Efficacy and Tolerance of Honey-impregnated Dressings in the Local Management of Pressure Ulcers
Condition: Pressure Ulcer
Interventions: Device: MELECTIS G;   Procedure: Usual care
17 Recruiting Adipose-Derived Stromal Cells (ASC's) and Pressure Ulcers
Condition: Pressure Ulcer
Interventions: Biological: Adipose-derived stromal cells;   Drug: Placbo
18 Recruiting Assessment of the Potential for Pressure Ulcer Formation
Condition: Pressure Ulcer Not Visible
Intervention: Other: Spatial Frequency Domain Imaging
19 Not yet recruiting Impact of the Use of Dressings Versus Lubrication of Skin With Cream to Prevent Pressure Ulcers: Clinical Trial
Condition: Pressure Sore
Intervention: Device: Hydrocolloid Dressing of Skin
20 Not yet recruiting Comparison of 2 Mattresses for the Prevention of Bedsores by Measuring Skin Pressure in the Sacral Area
Condition: Pressure Ulcer
Interventions: Device: AIRSOFT DUO for 1 day;   Device: SENTRY 1200 for 1 month;   Device: SENTRY 1200 for 1 day;   Device: AIRSOFT DUO for 1 month

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Study has passed its completion date and status has not been verified in more than two years.