PRAETORIAN: Prospective Real-world Registry Describing Treatment Regimens

Sponsor
Assistance Publique Hopitaux De Marseille (Other)
Overall Status
Recruiting
CT.gov ID
NCT03942913
Collaborator
(none)
573
1
50.7
11.3

Study Details

Study Description

Brief Summary

This study is to describe the initial anti-thrombotic treatment strategy prescribed to the AF patient population undergoing PCI by using drug class description.

Condition or Disease Intervention/Treatment Phase
  • Other: an observational study

Detailed Description

Coordinator of project has strong expertise in cardiovascular research and especially in ACS, PCI and antiplatelet therapy. The group led by pr Bonello has published several articles (appendix 3) including the VASP studies which have been presented at major cardiologic congresses (late breaking trials ACC 2007, AHA 2008, TCT 2011, EuroPCR 2010) including physicians and biologists. The group is composed of international experts in this research field (Pr Bonello, Pr Cuisset, Dr Barragan, Pr Lemesle). Additionally, coordinator center has a strong expertise in clinical research and a methodological support will be provided by the

Clinical Research Platform of the AP-HM (responsible: Prof. Pascal Auquier, medical referent:

Dr Karine Baumstarck).

The project brings together investigators that have been previously involved in many clinical studies in the field of ACS and PCI. In particular they have joined forces on multicenter trials leaded by the cardiology department of the Hôpital Universitaire Nord de Marseille (the VASP studies, the Early clinical trial) and they have regular meetings to share scientific data and research program design and advancement. There is a good capacity and ability of recruitment by the partner centers. The procedures to perform in this project are very simple and the disease is frequent. These are good criteria for the feasibility.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
573 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Real-world Prospective Registry to Describe the Current Treatment Patterns With Oral Anticoagulant and Antiplatelet Agents Association in Patients With Atrial Fibrillation and Undergoing Percutaneous Coronary Intervention
Actual Study Start Date :
Oct 10, 2019
Anticipated Primary Completion Date :
Aug 1, 2023
Anticipated Study Completion Date :
Dec 31, 2023

Arms and Interventions

Arm Intervention/Treatment
dual therapy

including 1 antiplatelet treatment aspirin or clopidogrel associated with 1 anticoagulant treatment VKA or NOAC.

Other: an observational study
this study is to describe the initial anti-thrombotic treatment strategy prescribed to the AF patient population undergoing PCI by using drug class description.

triple therapy

including 2 antiplatelet treatments (aspirin and clopidogrel) associated with 1 anticoagulant treatment VKA or NOAC. In VKA class, 2 different drugs are commonly prescribed: warfarin and fluidinione. In NOAC class, 3 different drugs are commonly prescribed: rivaroxaban, apixaban, dabigatran.

Other: an observational study
this study is to describe the initial anti-thrombotic treatment strategy prescribed to the AF patient population undergoing PCI by using drug class description.

Outcome Measures

Primary Outcome Measures

  1. frequency of patients treated after PCI with each drug class. [1 year]

Secondary Outcome Measures

  1. The type, the daily dosage and the duration of each drug class [18 MONTHS]

  2. The type, the daily dosage and the duration of each drug combination [18 MONTHS]

  3. tthe type of bleeding events according TIMI classification1 for each drug [18 MONTHS]

  4. The major adverse cardiovascular events (MACE) [18 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Inclusion Criteria:
The eligible subjects must meet all of the following criteria:
  • Man or woman 18 years old or over

  • Subject requiring percutaneous coronary intervention according to physician's and with AF requiring chronic anticoagulation by dual therapy or triple therapy;

  • Subject with pulmonary embolism risk score > 1 for men and ≥ 1 for women in CHA2DS2-VASc classification

  • Subject having declare its non-opposition to study participation

Exclusion Criteria:
  • Child-bearing potential (1 year post-menopausal, contraceptive or surgically sterile)

  • Lactation

  • No health insurance

  • Prisoners

Contacts and Locations

Locations

Site City State Country Postal Code
1 Assistance Publique Hopitaux de Marseille Marseille France 13354

Sponsors and Collaborators

  • Assistance Publique Hopitaux De Marseille

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Assistance Publique Hopitaux De Marseille
ClinicalTrials.gov Identifier:
NCT03942913
Other Study ID Numbers:
  • 2019-20
  • 2019-A00325-52
First Posted:
May 8, 2019
Last Update Posted:
Aug 16, 2022
Last Verified:
Aug 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Aug 16, 2022