BACKGROUND:In most emergency situations or severe illness, patients are unable to consent for clinical trial enrollment. In such circumstances, the decision about whether to participate in a scientific study or not is made by a legally designated representative. OBJECTIVE:To address the willingness of patients admitted to the intensive care unit (ICU) to be enrolled in a scientific study as volunteers, and to assess the agreement between patients' and their legal representatives' opinion concerning enrollment in a scientific study. METHODS:This survey was conducted in two hospitals in São Paulo, Brazil. Patients (≥18 years) with preserved cognitive functions accompanied by a surrogate admitted to the ICU were eligible for this study. A surv...
Objective: To analyze the procedure of the informed consent for ICU research obtained before ICU adm...
INTRODUCTION: Alterations from first-party and surrogate decision-maker consent can enhance the feas...
The process of acquiring informed consents from patients belongs to one of the everyday activities o...
Background: In most emergency situations or severe illness, patients are unable to consent for clini...
Purpose: Critically ill patients are often unable to give informed consent to participate in clinica...
ObjectivesObtaining informed consent from patients in intensive care units (ICUs) prior to enrolment...
INTRODUCTION: Research in intensive care is necessary for the continuing advancement of patient care...
BackgroundAs critical care practice increases in scope, size, and complexity, enrollment of critical...
OBJECTIVES: To identify the proportion of critically ill patients able to consent to participation i...
International audienceClinical research remains a vital contributor to medical knowledge, and is an ...
International audienceOBJECTIVE: A European Union Directive provides for the designation of a surrog...
Data collection was conducted across three workstreams. In workstream (WS) 1, 17 ICU clinicians/rese...
Background Clinical research in severely ill or injured patients is required to improve healthcare b...
OBJECTIVES: Obtaining informed consent from patients in intensive care units (ICUs) prior to enrolme...
Objectives: 1) To establish within international and local ethical guidelines to obtain informed con...
Objective: To analyze the procedure of the informed consent for ICU research obtained before ICU adm...
INTRODUCTION: Alterations from first-party and surrogate decision-maker consent can enhance the feas...
The process of acquiring informed consents from patients belongs to one of the everyday activities o...
Background: In most emergency situations or severe illness, patients are unable to consent for clini...
Purpose: Critically ill patients are often unable to give informed consent to participate in clinica...
ObjectivesObtaining informed consent from patients in intensive care units (ICUs) prior to enrolment...
INTRODUCTION: Research in intensive care is necessary for the continuing advancement of patient care...
BackgroundAs critical care practice increases in scope, size, and complexity, enrollment of critical...
OBJECTIVES: To identify the proportion of critically ill patients able to consent to participation i...
International audienceClinical research remains a vital contributor to medical knowledge, and is an ...
International audienceOBJECTIVE: A European Union Directive provides for the designation of a surrog...
Data collection was conducted across three workstreams. In workstream (WS) 1, 17 ICU clinicians/rese...
Background Clinical research in severely ill or injured patients is required to improve healthcare b...
OBJECTIVES: Obtaining informed consent from patients in intensive care units (ICUs) prior to enrolme...
Objectives: 1) To establish within international and local ethical guidelines to obtain informed con...
Objective: To analyze the procedure of the informed consent for ICU research obtained before ICU adm...
INTRODUCTION: Alterations from first-party and surrogate decision-maker consent can enhance the feas...
The process of acquiring informed consents from patients belongs to one of the everyday activities o...