Se trata de un ensayo clínico multicéntrico, prospectivo, de fase II, aleatorizado, doble ciego con control simulado(placebo) para evaluar la eficacia y la seguridad del condicionamiento isquémico remoto (RIC) en pacientes con linfoma que vayan a recibir tratamiento quimioterápico con antraciclinas (al menos 5 ciclos).
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