Determinants of Oral Anticoagulants' Activity
NCT03172546 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 3
Last updated 2019-10-18
Summary
The primary objective of the present study is to determine the clinical, biological and genetic determinants of the anticoagulant activity in patients treated with either anti-IIa or anti Xa oral anticoagulants.
The secondary objective is to determine the clinical, biological or genetic determinants of hemorrhagic or thrombotic complications during a one year follow-up.
Results will lead to a better prediction of both drug response and risk of complications.
Conditions
- Anticoagulant
Interventions
- GENETIC
-
PK-PD genetic polymorphisms
PK-PD genetic polymorphisms analysis in patients receiving either anti-IIa or anti-Xa treatment
Sponsors & Collaborators
-
University Hospital, Lille
lead OTHER
Principal Investigators
-
Dominique Deplanque, MD, PhD · University Hospital, Lille
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-07-06
- Primary Completion
- 2019-10-15
- Completion
- 2019-10-15
Countries
- France
Study Locations
More Related Trials
-
Precision Medicine Platform for Novel Oral Anticoagulants
NCT04056143 ·Status: UNKNOWN
-
Pharmacogenetics of Acenocoumarol
NCT01492777 ·Status: COMPLETED
-
Efficacy and Safety of Low-molecular Weight Heparin for Thromboprophylaxis in Acutely Ill Medical Patients
NCT00311753 ·Status: COMPLETED ·Phase: PHASE3
-
The Association of Warfarin Dosage and Plasma Enantiomer Concentration With the Gene Polymorphisms of CYP and VKOR
NCT00247702 ·Status: UNKNOWN ·Phase: NA
-
Anticoagulation Length in Cancer Associated Thrombosis
NCT01817257 ·Status: TERMINATED ·Phase: PHASE2
-
The Study of Monitoring and Dosing Guidance of Direct Oral Anticoagulants Based on Pharmacokinetics, Pharmacodynamics, and Pharmacogenomics
NCT06362343 ·Status: RECRUITING
-
Thrombophilia Assessment Under DOAC: Effectiveness of Activated Charcoal
NCT06171984 ·Status: RECRUITING
-
A Pharmacogenetic Study of Warfarin Dosing, "The COUMA-GEN Study"
NCT00334464 ·Status: COMPLETED ·Phase: NA
-
A Nationwide Observational Study Looking at Effectiveness and Bleeding Complications of NOACs vs. VKA in Non-valvular Atrial Fibrillation Patients.
NCT03715725 ·Status: TERMINATED
-
Residual Anti-Xa Activity After Last Treatment Dose of Enoxaparin
NCT03296033 ·Status: TERMINATED ·Phase: PHASE4
-
Bleeding Risk Evaluation in Haemophilia Patients Under Antiplatelet Therapies
NCT03157154 ·Status: COMPLETED
-
Impact of Biomarkers on Pharmacokinetics and Pharmacodynamics of Direct Oral Anticoagulants
NCT03161496 ·Status: UNKNOWN
-
EUropean Pharmacogenetics of AntiCoagulant Therapy - Warfarin
NCT01119300 ·Status: COMPLETED ·Phase: PHASE4
-
PRospective Evaluation Comparing Initiation of Warfarin StrategiEs (PRECISE): Pharmacogenetic-guided Versus Usual Care
NCT00377143 ·Status: WITHDRAWN ·Phase: PHASE4
-
Study in Healthy Volunteers of the Reversion by Haemostatic Drugs of the Anticoagulant Effect of New Anti-thrombotics
NCT01210755 ·Status: COMPLETED ·Phase: PHASE4
-
Xarelto Regulatory Post-Marketing Surveillance
NCT01029743 ·Status: COMPLETED
-
Quality of Life and Efficacy Evaluation of Patient Self-monitoring Their Oral Anticoagulation Therapy
NCT01033279 ·Status: COMPLETED ·Phase: NA
-
Genetic Determinants of Warfarin Anticoagulation Effect
NCT00162435 ·Status: UNKNOWN ·Phase: NA
-
Evaluation of Anti-Xa Levels in Surgery Patients Receiving Fixed Dose Heparin
NCT02970032 ·Status: COMPLETED ·Phase: EARLY_PHASE1
-
Evaluation of the Predictive Value of the Microvesicle Coagulo-lytic Balance in the Recurrence of Venous Thrombosis
NCT03265054 ·Status: UNKNOWN
-
EUropean Pharmacogenetics of AntiCoagulant Therapy - Phenprocoumon
NCT01119274 ·Status: COMPLETED ·Phase: PHASE4
-
Pharmacogenomics of Anti-platelet Intervention-2 (PAPI-2) Study
NCT01452152 ·Status: TERMINATED ·Phase: PHASE4
-
Reversal of the Antithrombotic Action of New Oral Anticoagulants
NCT01478282 ·Status: UNKNOWN ·Phase: PHASE4
-
Apixaban Versus Rivaroxaban in Non Valvular Atrial Fibrillation
NCT06862726 ·Status: ENROLLING_BY_INVITATION ·Phase: PHASE4
-
A Open-label, Three-period, Partial-replicate Design Study to Evaluate the Inter- and Intrasubject Variability of the Avatrombopag To-be-marketed Formulation Administered as Single Doses of 40 mg to Healthy Subjects Receiving a Low-fat Meal
NCT01759394 ·Status: COMPLETED ·Phase: PHASE1