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Personalized Blood Thinner Treatment Advancing Care for Patients with Blood Clotting Disorders through Genetic Testing

Development and validation of a prediction model for personalized Newer Oral anticoagulant (NOAC) therapy in patients with thromboembolic events by integrating Pharmacogenomics and cost-effectiveness: A prospective Interventional study - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/12/077975
Enrollment
96
Registered
2024-12-11
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Health Condition 1: I634- Cerebral infarction due to embolism of cerebral arteries

Interventions

Intervention1: Apixaban 5mg tablet: Normal dose- Tablet Apixaban 5mg twice daily ( morning and night) after food. If Apixaban failure occurs, it will be changed to: Tab Dabigatran 150mg twice dai

Sponsors

Amrita Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Inpatients and outpatients of Department of Stroke medicine and Adult cardiology Patients with and without NOAC failure

Exclusion criteria

Exclusion criteria: History of any mechanical or prosthetic valve replacements Patients on haemodialysis or waiting for any renal replacement surgery Patients who are about to undergo any surgery Patients with congenital coagulation abnormalities Patients who are not willing to participate in the study Patients/caregivers who are unwilling to sign the informed consent Pregnant and lactating women

Design outcomes

Primary

MeasureTime frame
To determine the prevalence of single nucleotide polymorphisms (SNP) associated with ineffective drug response among patients receiving NOACs for anticoagulation therapy.Timepoint: Six months

Secondary

MeasureTime frame
To establish genetic profiling test for appropriate NOACs for thrombosis prevention with minimal adverse complications (effective NOAC based on individual genomic conditions). Timepoint: Six months;To identify key etiological factors for ineffective anticoagulation in patients taking NOAC. Timepoint: Six months;To assess a cost-effectiveness analysis of pharmacogenomic-guided dosing strategy.Timepoint: Baseline, 3months, 6 months & 1 year.

Countries

India

Contacts

Public ContactDr Chameli Ratan

Amrita Institute of Medical Sciences

dr.vivek.in@gmail.com8921485541

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026