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NCT03907046 · ClinicalTrials.gov registry record · Phase 3

Anticoagulation in ICH Survivors for Stroke Prevention and Recovery

A Phase 3 study of Atrial Fibrillation and Intracerebral Hemorrhage, sponsored by Yale University.

Recruiting
Registry status
Phase 3
Development phase
700
Enrollment target
20
Study locations

NCT03907046: Recruiting Phase 3 study of Atrial Fibrillation and Intracerebral Hemorrhage, sponsored by Yale University.

NCT03907046 is a Phase 3 study of Atrial Fibrillation and Intracerebral Hemorrhage that is actively recruiting participants, run by Yale University. The registered enrollment target is 700 participants, below the 2,993-participant average among 202 other Atrial Fibrillation trials with a reported enrollment target (77% lower). The trial reports 20 study locations across 4 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03907046, a Phase 3 study of Atrial Fibrillation and Intracerebral Hemorrhage, is actively recruiting participants, sponsored by Yale University.

RECRUITING
Registry status
Phase 3
Development phase
700 participants
Enrollment target
20
Study locations

Study Summary

Primary Aim: To determine if apixaban is superior to aspirin for prevention of the composite outcome of any stroke (hemorrhagic or ischemic) or death from any cause in patients with recent ICH and atrial fibrillation (AF). Secondary Aim: To determine if apixaban, compared with aspirin, results in better functional outcomes as measured by the modified Rankin Scale.

Primary Outcome

Incidence of stroke of any type (ischemic or hemorrhagic) or death from any cause

Interventions

  • DRUG Aspirin
  • DRUG Apixaban

Study Locations (20)

California

  • Mercy San Juan Medical Center - Carmichael
  • Eden Medical Center, Castro Valley - Castro Valley
  • Arrowhead Regional Medical Center - Colton
  • Rancho Los Amigos National Rehabilitation Center - Downey
  • Kaiser Permanente Fontana Medical Center - Fontana
  • Community Regional Medical Center of Fresno - Fresno
  • St. Jude Medical Center - Fullerton
  • Long Beach Memorial Medical Center - Long Beach
  • Los Alamitos Medical Center - Los Alamitos
  • Kaiser Permanente Los Angeles Medical Center - Los Angeles
  • Cedars-Sinai Medical Center - Los Angeles
  • Ronald Reagan UCLA Medical Center - Los Angeles
  • Doctors Medical Center Modesto, Modesto, CA - Modesto
  • Hoag Hospital Newport Beach - Newport Beach

Arizona

  • Chandler Regional Medical Center - Chandler
  • St. Joseph's Hospital and Medical Center - Phoenix
  • Banner University Medical Center - Tucson

Alabama

  • University of Alabama Hospital - Birmingham
  • University of South Alabama University Hospital - Mobile

Arkansas

  • UAMS Medical Center - Little Rock

Trial Details

FieldValue
Enrollment Target 700 participants
Start Date 2020-01-28
Est. Completion 2027-04
Phase Phase 3
Yale University

1,492 total trials

What NCT03907046 shows while recruiting

NCT03907046 is an interventional study that assigns participants to a tested intervention. The registered 700 participants enrollment target is mid-sized for trials with a published cap, below the 2,993-participant average among 202 other Atrial Fibrillation trials with a reported enrollment target (77% lower).

The record links to 2 conditions, with Atrial Fibrillation appearing as the primary indexed condition, and to 2 interventions - of which Aspirin is the first listed.

NCT03907046 names 20 study sites across 4 states, led by California, Arizona, Alabama.

Frequently Asked Questions

What is clinical trial NCT03907046 about?

NCT03907046 is a clinical study titled "Anticoagulation in ICH Survivors for Stroke Prevention and Recovery". Primary Aim: To determine if apixaban is superior to aspirin for prevention of the composite outcome of any stroke (hemorrhagic or ischemic) or death from any cause in patients with recent ICH and atrial fibrillation (AF). Secondary Aim: To determine if apixaban, compared with aspirin, results in b...

What is the current status of trial NCT03907046?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 700 participants. The study started on 2020-01-28. Estimated completion is 2027-04.

What conditions does trial NCT03907046 study?

This clinical trial studies the following conditions: Atrial Fibrillation, Intracerebral Hemorrhage.

What interventions are being tested in trial NCT03907046?

The interventions under investigation include: Aspirin (DRUG), Apixaban (DRUG).

Who is sponsoring clinical trial NCT03907046?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03907046 being conducted?

This trial has 20 study locations across Alabama, Arizona, Arkansas, California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Atrial Fibrillation

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT03907046's enrollment target sits among peer trials

700 43rd of 202 higher than 160 of 202 other Atrial Fibrillation trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Atrial Fibrillation trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03907046, the US trial registry maintained by the National Library of Medicine. NCT03907046 (mid enrollment · wide site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.