Conducting Randomized Trials in the Prehospital Setting

Michael R. Sayre; Marianne Gausche‐Hill

doi:10.3109/10903120209102681

January 1, 2002Prehospital Emergency Care

Conducting Randomized Trials in the Prehospital Setting

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Key Points

To review the methodological, logistical, and regulatory frameworks required to successfully execute randomized clinical trials within emergency medical services.
Methodological overview evaluating protocol design, patient enrollment, and practical barriers unique to prehospital interventions.
Assessment of regulatory standards, including exception from informed consent in emergency research settings.
Identifies key obstacles in prehospital research, including rapid patient triage, provider training, and time-critical drug or device administration.
Outlines implementation paradigms that balance rigorous experimental controls with standard emergency operational workflows.

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Implication

Review outlines operational and methodological strategies for clinical trials in emergency medical services, highlighting approaches to optimize prehospital study design.

Abstract

(2002). Conducting Randomized Trials in the Prehospital Setting. Prehospital Emergency Care: Vol. 6, No. sup2, pp. S38-S47.

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Sayre et al. (2002) studied this question.

synapsesocial.com/papers/6a7bfc3b1f8f1eb7b8ed49c8 https://doi.org/10.3109/10903120209102681

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Conducting Randomized Trials in the Prehospital Setting

Key Points

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Implication

Abstract

Discussion

Cite This Study

Conducting Randomized Trials in the Prehospital Setting

Key Points

Ask about this paper

Implication

Abstract

Discussion

Cite This Study

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