{"id":7698,"date":"1995-01-01T00:00:00","date_gmt":"1995-01-01T00:00:00","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/1995\/01\/01\/diseno-y-evaluacion-de-un-ensayo-de-bioequivalencia-de-comprimidos-de-ciprofloxacino\/"},"modified":"1995-01-01T00:00:00","modified_gmt":"1995-01-01T00:00:00","slug":"diseno-y-evaluacion-de-un-ensayo-de-bioequivalencia-de-comprimidos-de-ciprofloxacino","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/ciencias-medicas\/diseno-y-evaluacion-de-un-ensayo-de-bioequivalencia-de-comprimidos-de-ciprofloxacino\/","title":{"rendered":"Dise\u00f1o y evaluacion de un ensayo de bioequiValencia de comprimidos de ciprofloxacino."},"content":{"rendered":"<h2>Tesis doctoral de <strong>  Rosique Robles Juan a Dolores <\/strong><\/h2>\n<p>Se realiza un ensayo de bioequiValencia de dos marcas registradas de comprimidos de ciprofloxacina 500 mg:  baycip y cunesin, en 14 voluntarios sanos y con un dise\u00f1o cruzado. Se calculan los parametros que caracterizan la biodisponibilidad en magnitud: auc, y en velocidad: cmax y tmax, y se analiza la bioequiValencia mediante la comparacion de las diferencias, y cocientes, de los parametros obtenidos con el medicamento problema (cunesin() y de referencia (baycip). Como criterios de bioequiValencia, se utilizan el 80-125%; el 70-130% y el tmax +- 0.5 horas, y, como tratamientos estadisticos, el intervalo de confianza clasico, el procedimiento de schuirmann, el metodo de rodda y davis, y el intervalo de confianza no parametrico. Asimismo, se ha caracterizado el modelo y los parametros farmacocineticos individuales y poblaciones del farmaco.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Dise\u00f1o y evaluacion de un ensayo de bioequiValencia de comprimidos de ciprofloxacino.<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Dise\u00f1o y evaluacion de un ensayo de bioequiValencia de comprimidos de ciprofloxacino. <\/li>\n<li><strong>Autor:<\/strong>\u00a0  Rosique Robles Juan a Dolores <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Universitat de val\u00e9ncia (estudi general)<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 01\/01\/1995<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<h3>Direcci\u00f3n y tribunal<\/h3>\n<ul>\n<li><strong>Director de la tesis<\/strong>\n<ul>\n<li> Casabo Alos Vicente G.<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal:  Pla Delfina  Jos\u00e9 M <\/li>\n<li>Jos\u00e9 Martinez Lanao (vocal)<\/li>\n<li>Esteban Morcillo Sanchez (vocal)<\/li>\n<li>Jos\u00e9 Domenech Berrozpe (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Rosique Robles Juan a Dolores Se realiza un ensayo de bioequiValencia de dos marcas registradas de comprimidos [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center 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