Viewing Study NCT00227097



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Last Modification Date: 2024-10-26 @ 9:19 AM
Study NCT ID: NCT00227097
Status: TERMINATED
Last Update Posted: 2006-07-07
First Post: 2005-09-23

Brief Title: EducAvk Recommendations for the Antivitamin Ks Gestion
Sponsor: University Hospital Grenoble
Organization: University Hospital Grenoble

Study Overview

Official Title: Implication of Patient in the Making Ready of Recommendations for the Antivitamin Ks Gestion in Case of Thrombosis Embolic Venouss Illness Randomised Study for Clinical Validation
Status: TERMINATED
Status Verified Date: 2006-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The objective of the project EducAvk is to document the efficacy of a strategy combining a specific follow up-notebook and education of attending patient with a pedagogic support comparatively to an usual education on the impact of clinical events at three months minor or major hemorrhagic events recurrence of thrombi-embolics disease
Detailed Description: Standard strategies for the implementation of recommendations are exclusively focused on practitioners But often they do not appear to be effective insufficient time accorded per patient lack of training

However some qualitative surveys have shown the benefit of a greater role on the part patient in the process of transmitting recommendations through the practitioner

In this study patient education is begun by the angiologist or a pharmacy student under the responsibility of the hospital investigator Follow-up is realized by the patients general practitioner

More patient involvement in the realization of the recommendations could increase the proportion of practitioners who follow the recommendations and decrease the iatrogenicity of antivitamin K AVK

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None