Clinical Trials Directory

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UnknownNCT06057467

Early Versus Late Initiation of Anticoagulation in Mild-to-moderate AIS Patients With NVAF

Early Versus Late Initiation of Anticoagulation in Mild-to-moderate Acute Ischemic Stroke Patients With Non-valvular Atrial Fibrillation

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
2,351 (estimated)
Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this clinical trial is to compare the effectiveness between early and late initiation of anticoagulation therapy in acute ischemic stroke (AIS) patients with non-valvular atrial fibrillation (NVAF). Participants will be 1:1 randomized into early or late initiation group. The primary endpoint is early neurological deterioration (END) before discharge.

Detailed description

Anticoagulation therapy is effective to prevent ischemic stroke in patients with NVAF who have a history of stroke. Recent clinical trials have demonstrated that early initiation of anticoagulation therapy after AIS is safe, while no remarkable benefits have been observed. The goal of this clinical trial is to compare the effectiveness between early and late initiation of anticoagulation therapy in AIS patients with non-NVAF. Participants will be 1:1 randomized into early or late initiation group. The primary endpoint is END before discharge.

Conditions

Interventions

TypeNameDescription
DRUGAnticoagulation AgentsAnticoagulation agents includes rivaroxaban, dabigatran, apixaban, and edoxaban.

Timeline

Start date
2023-09-15
Primary completion
2025-10-01
Completion
2026-01-01
First posted
2023-09-28
Last updated
2024-03-18

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT06057467. Inclusion in this directory is not an endorsement.