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Study identifier: NCT06819943 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Effectiveness of Platform-Based Lateralization Therapy in Reducing Interface Pressure Between The Patient And The Support Surface

Condition: Respiratory Insufficiency · Pressure Injury · Intensive Care Medicine  ·  Sponsor: University of Sao Paulo General Hospital

PhaseNA
Planned participants25
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Pressure injury (PI) is characterized as damage to the skin and/or underlying tissues resulting from sustained pressure or a combination of pressure and shear forces between the patient and the support surface. Prolonged pressure is a well-established risk factor in the development of PIs. Frequent repositioning and routine patient care have been recognized for decades as integral components of PI prevention and treatment protocols. The duration of interface pressure is as critical as its magnitude. When interface pressure exceeds the mean capillary blood pressure, blood flow can be compromised, leading to ischemia in affected areas, which may progress to necrosis if sustained over time. Furthermore, it is widely accepted in the literature that tissue becomes at risk when interface pressure exceeds 30 to 32 mmHg. In this context, continuous lateral rotation therapy (CLRT) offers a potential alternative for managing critically ill patients. CLRT involves continuous mechanical rotation of the patient in the lateral plane. However, its effects on skin integrity remain poorly understood. Despite the rationale behind and widespread recommendation of repositioning, the lack of robust evaluations on how repositioning impacts interface pressure creates uncertainty, underscoring the need for high-quality trials to assess different strategies for implementation. Although lateralization is a pragmatic strategy for preventing pressure injuries, its use in critically ill patients requi…

This description comes directly from the study's public registry record.

Talk to the study team

Marcelo BP Amato, MD PhD  ·  +55113061-7361  ·  marcelo.amato@hc.fm.usp.br

Anne C Almeida de Sousa, PT  ·  +5579998577249  ·  anne.sousa@usp.br

Always discuss trial participation with your own doctor first.

Locations (1)

Instituto do Coração do Hospital das Clínicas da Faculdade de Medicina da Universidade São PauloSão Paulo, São Paulo, BrazilRecruiting

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Source record: clinicaltrials.gov/study/NCT06819943