Clinical Trials Logo

Clinical Trial Summary

Introduction: A side-lying recovery position is recommended when victims are unresponsive but breathing normally and, hence, do not require cardiopulmonary resuscitation. In 2021, the European Resuscitation Council (ERC) and the Belgian Red Cross-Flanders issued new guidelines which included the description of a modified recovery position to avoid problems in victims with joint stiffness and to overcome potential obstructed venous return in the dependent arm. Based on good practice insights, the dependent arm will now be extended and not bent to support the other arm. However, there is currently no evidence available to support a specific recovery position. Objectives: The aim of this study is to assess the impact of different recovery positions on perfusion of the forearm and associated comfort. Methods: In this cross-over randomized controlled trial, 24 healthy volunteers will be placed in either the lateral recovery position with extended dependent arm or with bent arm, and in the other position thereafter. Before and between both recovery positions, the volunteers will be positioned supine for 15 min. Several perfusion indices of the forearm will be non-or mildly invasively monitored in the respective recovery positions by radial artery tonometry, ulnar artery echo doppler and venous congestion plethysmography. Subjective participant's discomfort and pain will be assessed as well. Differences in continuous outcomes between the different recovery positions will be assessed with paired t-tests or wilcoxon signed-rank test. Discussion: The benefit of lateral positioning of adults and children with decreased level of consciousness has been widely accepted despite limited supportive scientific evidence. We here will provide direct evidence (i) whether venous drainage in the dependent limb is impaired when positioning the victim in the lateral recovery position with bent arms and (ii) whether this potential complication can be minimized by extending the dependent arm. The major limitations of this study is that healthy volunteers, instead of non-responsive victims, are included as participants, and that the study will be performed in a highly controlled environment. Nevertheless, the generated insights will directly fuel evidence-based treatment recommendations regarding the recovery position in first aid settings, and fill a current gap in evidence.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05587179
Study type Interventional
Source Centre for Evidence-Based Practice, Belgium
Contact
Status Completed
Phase N/A
Start date December 21, 2022
Completion date October 31, 2023

See also
  Status Clinical Trial Phase
Completed NCT01011192 - Performance of Two Different ke0s in the Same Pharmacokinetic Propofol Model N/A
Not yet recruiting NCT06036732 - A New Approach in Intensive Care Unit Consciousness Assessment: FIVE Score
Completed NCT03913065 - Head Computed Tomography for Predicting Neurological Outcome After Cardiac Arrest
Completed NCT03290859 - Race-Specific Propofol Titration to Effect for Procedural Sedation
Completed NCT03699306 - Comparison of Three Methods for NG Tube Placement N/A
Completed NCT02624401 - The Neural Mechanisms of Anesthesia and Human Consciousness (Part 6) Phase 4
Withdrawn NCT01730001 - Early Versus Late Intubation Trial in Physician Manned Emergency Medical Services N/A
Completed NCT05496985 - Chinese Validation of the Simplified Evaluation of CONsciousness Disorders(SECONDs) N/A
Completed NCT03284307 - UNderstanding CONSciousness Connectedness and Intraoperative Unresponsiveness Study Phase 4