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NCT03304977 Clinical Trial

Patient's Knowledge on Their Anticoagulating and Anti Platelet Treatment St Joseph's Hospital)

Coagulation Disorder Clinical Trial

Official title:
Current Situation of the Patient's Knowledge on Their Anticoagulating and Anti Platelet Treatment in GHPSJ (St Joseph's Hospital)

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03304977
Other study ID # CACHACA
Secondary ID
Status Completed
Phase N/A
First received September 29, 2017
Last updated October 3, 2017
Start date June 6, 2016
Est. completion date October 30, 2016

Study information
Verified date September 2017
Source Groupe Hospitalier Paris Saint Joseph
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Oral antigoagulant are used more than 60 years in thrombotic diseases. Even they are indispensable, the haemorragic risk is high.That's why it's the main reason of hospitalization for iatrogeny.The complication's reasons are mainly linked to errors of drug intake, drugs interaction and the lack of understanding the treatment.Moreover, the antiplatelet agglutening treatment is frequently added to anticoagulant treatment.This increases the haemorragic risk.Different means were used to minimize the risk , like INR follow up.

The purpose of the study is to evaluate smartphone use to follow the patients'treatment.

Description:

Two questionnaire via smartphone with 15 days gap.

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date October 30, 2016
Est. primary completion date July 31, 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patient under ant-thrombotic treatment

- hospitalized in vascular medecine service

Exclusion Criteria:

- refusing the participation

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• questionnaire via smartphone
questionnaire via smartphone

Locations
Country Name City State
France Groupe Hospitalier Paris Saint Joseph Paris Ile-de-France

Sponsors (1)
Lead Sponsor Collaborator
Groupe Hospitalier Paris Saint Joseph

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary smartphone use level evaluation of the interest of patient to use their smartphone in the purpose to follow their anticoagulant treatment 15 days
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