Vascular Diseases Clinical Trial
— APPLIACOfficial title:
Study of the Interest of Patients Undergoing Anti-thrombotic Treatment in a Digital Application of Therapeutic Assistance
Verified date | October 2022 |
Source | Groupe Hospitalier Paris Saint Joseph |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Medical ethics encourages medical personal to actively care for patients, however old they may be, if they have maintained their physical autonomy and mental integrity to travel the path of medical care together. Many of the patients are in this situation today and their age does not seem to be a limiting factor in the care required. For more than 60 years, antithrombotics have played a major role in the management of thromboembolic and arterioatheromatous diseases. the doctors have therefore seen the advent of low molecular weight heparins, new platelet antiaggregants and then direct oral anticoagulants. If their contribution is no longer discussed today, it is necessary to take into consideration the risks they cause, particularly in terms of haemorrhage. Indeed, antithrombotics are the leading cause of serious adverse reactions in France with anti-vitamins K (AVK) which are the leading cause of hospitalization for severe iatrogeny in France. This risk is increased by the coexistence of haemorrhagic risk factors: drug interaction, misuse, failure to comply with contraindications and precautions for use, especially as exposure to these drugs increases with age.
Status | Terminated |
Enrollment | 25 |
Est. completion date | October 10, 2022 |
Est. primary completion date | October 10, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Patient = 18 years old - Patient hospitalized in the vascular medicine department of the GHPSJ or attending a general medical consultation at the CMT - Patient with at least one vascular pathology: pulmonary embolism, venous thrombosis or phlebitis, cardiac arrhythmia by atrial fibrillation, obliterating arteriopathy of the lower limbs or myocardial infarction - Patient on antithrombotic treatment[anticoagulants : AVK or Anticoagulants Oraux Directs (AOD), or antiplatelet agents] - Patient affiliated to a health insurance plan - Patient able to read and understand the French language - Patient capable of giving free, informed and express consent Exclusion Criteria: - Patient not residing in Ile de France - Patient whose investigator considers that he/she is not able to use a digital tablet - Patient deprived of liberty - Patient under guardianship or curatorship - Refusal to participate in the study - Patient judged not to be included by the investigator on the basis of the inclusion questionnaire |
Country | Name | City | State |
---|---|---|---|
France | Groupe Hospitalier Paris Saint-Joseph | Paris |
Lead Sponsor | Collaborator |
---|---|
Groupe Hospitalier Paris Saint Joseph |
France,
Dahri K, Loewen P. The risk of bleeding with warfarin: a systematic review and performance analysis of clinical prediction rules. Thromb Haemost. 2007 Nov;98(5):980-7. Review. — View Citation
Linkins LA, Choi PT, Douketis JD. Clinical impact of bleeding in patients taking oral anticoagulant therapy for venous thromboembolism: a meta-analysis. Ann Intern Med. 2003 Dec 2;139(11):893-900. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Return of the tablet in working order and to its use | return (yes/no) and use | 1 month | |
Secondary | Number of pages consulted on the educational tablet | 1 month | ||
Secondary | Analyses of patient treatment knowledge assessment questionnaires | The two questionnaires contain 12 and 11 questions respectively. the possible answers are yes or no | Day 0 - 1 month | |
Secondary | Analogical visual scale of patient satisfaction | Analogical visual scale of patient satisfaction from minimum 0 (very satisfied) to maximum 10 (not satisfied) | 1 month | |
Secondary | Questionnaire on compliance with antithrombotic treatments on application | taking antithrombotic treatments (yes/no) | 1 month | |
Secondary | Reporting of adverse events via the dedicated field on the educational tablet | 1 month | ||
Secondary | Number of calls from city physicians and pharmacists received by the investigator | 1 month |
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