ClinicalTrials.gg
CompletedNCT03304977Updated Oct 9, 2017

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

An interventional study of questionnaire via smartphone in Coagulation Disorder, sponsored by Fondation Hôpital Saint-Joseph. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-10-09.

Sponsored by Fondation Hôpital Saint-Joseph · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 1 year 3 months after the study started (first participant enrolled Jun 2016, registered Sep 2017).
Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study 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.

Read the detailed description

Two questionnaire via smartphone with 15 days gap.

02

Conditions studied

  • Coagulation Disorder

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03

In context

Hemostatic Disorders

515 studies on the registry are indexed under Hemostatic Disorders; 72 are open to participants now.

This study's enrollment of 100 is above the median of 52 across 261 interventional studies indexed under Hemostatic Disorders.

Browse Hemostatic Disorders studies →

Lead sponsor

Fondation Hôpital Saint-Joseph is the lead sponsor of 344 studies on the registry; 49 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • patient under ant-thrombotic treatment
  • hospitalized in vascular medecine service

Exclusion criteria

Exclusion Criteria:

  • refusing the participation
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
100 participants (actual)

Interventions

  • Otherquestionnaire via smartphone

    questionnaire via smartphone

06

What researchers measure

Primary outcomes

  1. smartphone use level

    evaluation of the interest of patient to use their smartphone in the purpose to follow their anticoagulant treatment

    Time frame: 15 days

07

Study locations

1 site
  • Groupe Hospitalier Paris Saint Joseph
    Paris, Île-de-France Region 75014, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 9, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03304977
Responsible party
Sponsor
First posted
Oct 9, 2017
Start date
Jun 6, 2016
Primary completion
Jul 31, 2016
Completion
Oct 30, 2016
Last update
Oct 9, 2017

Study contacts

Pascal PRIOLLET, MD
study director · GHPSJ

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2017. You cannot join it, but the record below documents what was studied.

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Discussion

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