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What Treatment for Patients With Phlebitis or Pulmonary Embolism ?

Patients' Choice in Terms of Anticoagulant Therapy in Venous Thrombo- Embolism Disease. AntiCoagChoice Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03889457
Acronym
AntiCoagChoice
Enrollment
1000
Registered
2019-03-26
Start date
2019-02-12
Completion date
2021-02-12
Last updated
2019-03-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Venous Thrombosis or Pulmonary Embolism

Keywords

Deep Vein Thrombosis, Superficial Vein Thrombosis, Anticoagulant, Patient Compliance, Preference, Venous Thrombosis, pulmonary embolism

Brief summary

The objective of the anticoagchoice study is to analyze the preferences of people suffering from phlebitis, in terms of anticoagulant, to improve adherence to these treatments, to adapt the medical prescriptions.

Detailed description

Venous thromboembolism (VTE) is the third leading cause of cardiovascular death, with an increase in annual incidence with age. With the advent of direct oral anticoagulants, the management of deep vein thrombosis and pulmonary embolism has evolved in recent years and these treatments are widely prescribed. There are studies comparing the different anticoagulant treatments used in venous thrombosis, which show no inferiority of treatment (injectable or oral) compared to others. Drug delivery modalities have been shown to affect adherence, and thus treatment efficacy. It seems fundamental to focus on patients' drug preferences in VTE to ensure the best possible compliance. These preferences seem to depend on the personal history of each patient. In addition, no studies have been conducted on patient preferences for anticoagulant therapy for VTE: this is the goal of the anticoagchoice study.

Interventions

OTHERanticoagulation choice

Type of anticoagulant chosen by the patient (oral or injectable).

Sponsors

SFMV (French Society of Vascular Medicine)
CollaboratorUNKNOWN
Rennes University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with deep vein thrombosis, superficial vein thrombosis, muscle vein thrombosis or pulmonary embolism, over 18 years of age. No

Design outcomes

Primary

MeasureTime frameDescription
The primary objective of this study is to analyze patient treatment preferences in venous thromboembolic disease.the time required for a consultation: 30 minutesThe primary outcome: To compare the proportion of patients choosing oral anticoagulation vs patients choosing injectable route.

Secondary

MeasureTime frameDescription
compare patients choosing oral anticoagulation vs patients choosing an injectable routethe time required for a consultation: 30 minutesproportions of patients choosing an oral anticoagulation vs. patients choosing an injectable pathway depending on the duration of treatment (3 months, 6 months or more),

Countries

France

Contacts

Primary ContactCecile Ferragu
cecile.ferragu@chu-rennes.fr02 99 28 25 55
Backup Contactdirection de la recherche clinique
drc@chu-rennes.fr02 99 28 25 55

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026