October 1, 2019 posted by

Nombre de los medicamentos: Genérico y Comercial – Aprenda acerca de las causas, los síntomas, el diagnóstico y el tratamiento de los Manuales MSD. Se ha demostrado que los antibióticos aplicados en el párpado alivian los síntomas y resuelven la infección bacteriana de los párpados. Contraindicadas en casos de hipersensibilidad a cualquiera de los antibióticos del grupo de la neomicina (aminoglucósidos), ya que existe sensibilización.

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Clear advanced search filters. Have known or suspected intolerance or hypersensitivity to the investigational product, closely related compounds, or any of the stated ingredients. The key secondary objective of this study is to evaluate the efficacy of SHP based on bacterial eradication defined as absence of all bacterial species present at or above pathological threshold at baseline compared with placebo in the treatment of subjects with bacterial conjunctivitis in the study eye at Visit 3 Day 5.

Uso de medicamentos de rescate. Full list of Exclusion criteria can be found in the protocol. Neonates or infants ie. Presence of any significant ophthalmic condition eg, Retinopathy of Prematurity, congenital cataract, congenital glaucoma or other congenital disorder with ophthalmic involvement that could affect study variables.

Age, sex, causes of eye loss, affected eye, conjunctival disease, type of cavity, length of time of prosthesis use, microbiological result, hygienic handling and response to treatment were the analyzed variables.

Derribando mitos: se puede tomar alcohol con la mayoría de los antibióticos | Futuretech

Use of rescue medication Safety Endpoints: Quantitaty eye lid evaluation of anophthalmic cavity carriers with external ocular prosthesis. Title of the trial for lay people, in easily understood, i.


Allergic conjunctivitis and conjunctival retraction are the most frequent illnesses in the patients wearing ocular prosthesis for more than one year, due to Staphylococcus aureus presence resulting from frequent hygienic handling of the prosthesis. Date on which this record was first entered in the EudraCT database:.

Sujetos de cualquier edad en la visita 1 Nota: Have presence of any intraocular, corneal, or conjunctival ocular inflammation eg, uveitis, iritis, ulcerative keratitis, chronic blepharoconjunctivitisother than bacterial conjunctivitis.

Bacterial eradication status defined as absence of all bacterial species present at or above pathological threshold at baseline as assessed by bacterial culture at Visits 2 Day 34 Day 8and 5 Day 12 in the study eye 4.

Key Secondary Efficacy Endpoints: Nicodemo D, Ferreira LM. For these items you should use the filters and not add them to your search terms in the text field. Combination product that includes a device, but does not involve an Advanced Therapy. Plans for treatment or care after the subject has ended the participation in the trial if it is different from the expected amtibioticos treatment of that condition. Both Female Only Male Only.

IMP with orphan designation in the indication.

Clinical trials

Tener una enfermedad ocular significativa p. Presence of nasolacrimal duct obstruction at Visit 1 Day 1.

Full list of Inclusion criteria can be found in the protocol. Time to clinical resolution based upon assessments at Visits 2 Day 33 Day 54 Day 8and 5 Day 12 oftapmicos the study eye 9. Las secreciones toman por esta causa un color verde-azuloso.


Indice multientrada

Have a clinical diagnosis of suspected bacterial antbioticos in at least 1 eye confirmed by the presence of the following oftalmidos clinical signs and symptoms in that same eye: The majority of patients positively responded to treatment. Definition of the end of the trial and justification where it is not the last visit of the last subject undergoing the trial.

How to search [pdf]. Current or relevant history of physical or psychiatric illness, any medical disorder that may make the subject unlikely to fully complete the study, or any condition that presents undue risk from the investigational product or procedures.

Have a preplanned overnight hospitalization during the period of the study. Expanded clinical resolution status, defined as a global clinical score of 0, 1, or 2 with neither injection nor discharge antibiotico a score of 2, at Visits 2 Day 33 Day 54 Day 8and 5 Day 12 in the study eye 8.

Questionnaire of the psychosocial profile of the patient with anophthalmia with indication of oftalicos prosthesis. Bacterial eradication status defined as absence of all bacterial species present at or above pathological threshold at baseline in the study eye at Visit 3 Day 5 between SHP and placebo. Trials with results Trials without results.