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Gastrointest Endosc Clin N Am ; 27(2): 327-341, 2017 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-28292410

RESUMEN

The recent increase in US Food and Drug Administration-approved weight-loss devices has diversified obesity treatment options. The regulatory pathways for endoscopically placed weight-loss devices and considerations for clinical trials are discussed, including the benefit-risk paradigm intended to aid in weight-loss-device trial development. Also discussed is the benefit-risk analysis of recently approved endoscopic devices. A strategic priority of the FDA Center for Devices and Radiological Health is to increase the use of patient input in decision making. Thus, we consider how endoscopic weight-loss devices with profiles similar to those that have been approved may be viewed in a patient preference study.


Asunto(s)
Cirugía Bariátrica/instrumentación , Aprobación de Recursos , Endoscopía Gastrointestinal/instrumentación , Obesidad/cirugía , Cirugía Bariátrica/legislación & jurisprudencia , Toma de Decisiones , Endoscopía Gastrointestinal/legislación & jurisprudencia , Humanos , Prioridad del Paciente , Estados Unidos
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