Impact of Anticoagulation Therapy on the Cognitive Decline and Dementia in Patients With Non-Valvular Atrial Fibrillation

Dementia Clinical Trial

— CAF  

Official title:

Impact of Anticoagulation Therapy on the Cognitive Decline and Dementia in Patients With Non-Valvular Atrial Fibrillation (CAF Trial)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03061006
• Other study ID #: 1050164
• Status: Completed
• Phase: Phase 4
• Start date: April 3, 2017
• Est. completion date: March 15, 2021

Study information

• Verified date: August 2021
• Source: Intermountain Health Care, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Patients will be screened at Intermountain Medical Center and at Intermountain-affiliated anticoagulation clinics in the Salt Lake City region. Patients with non-valvular atrial fibrillation will be considered for study. After written informed consent is obtained, subjects who meet eligibility criteria will be randomized 1:1 to 2 treatment arms: Group 1: Dabigatran etexilate (150 mg BID if CrCL > 30 mL/min, or 75 mg BID if CrCL > 15 to 30 mL/min or per USPI; and Group 2: Warfarin (Dose-adjusted (INR 2.0 - 3.0). Assessment of kidney function every 6 months will be done for Group 1. Standard warfarin follow-up and education, based upon system criteria, will be done for Group 2. All subjects will be followed for 24 months, and will be assessed at 1-week, then 3-, 6-, 12-, 18- and 24-months post-anticoagulation visits as well as other visits deem necessary for clinical care. All subjects will undergo protocol-specified laboratory tests and will complete 6 standard, validated questionnaires at each follow-up visit following the week 1 visit, except at the 3-month visit when only one questionnaire will be administered. To determine brain volume and characteristic changes representative of micro-bleeding, the first 10 subjects in each treatment group who are willing and able to undergo the procedure will participate in a MRI sub-study. The cranial MRI will be done at baseline and at 24-months post-anticoagulation on this sub-group.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 101
• Est. completion date: March 15, 2021
• Est. primary completion date: March 15, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 65 Years and older

Eligibility

Inclusion Criteria:

1. Male or female >65 years of age.

2. Non-valvular atrial fibrillation documented by electrocardiogram, ambulatory event monitor, or telemetry within 12 months of enrollment.

3. Moderate risk of thromboembolism based upon a CHADS score or CHADS2 Vasc score of =2.

4. Ability to complete a mini-mental status evaluation.

5. Ability to independently comprehend and complete a quality of life and dementia questionnaires.

6. Ability to provide informed consent for study participation.

7. Willing and able to comply with the prescribed follow-up tests and schedule of evaluations.

Exclusion Criteria:

1. Inability to take an anticoagulant due to known or perceived bleeding risk.

2. Known coagulopathy that may impact the choice, duration, efficacy and safety of anticoagulation therapy.

3. Atrial Fibrillation in the setting of valvular heart disease. Valvular heart disease defined as any surgical valve, mitral stenosis, or moderate-severe valvular heart disease.

4. Severe renal dysfunction, defined as a creatinine clearance rate <15 mL/min (documented within the last 3 months).

5. History of any form of dementia.

6. A life expectancy less than 24 months.

7. Inability to comply with the follow-up schedule.

8. Current participation in a clinical investigation that includes an active pharmacologic treatment arm.

9. An upper age limit not to be used if participation inclusion criteria are met.

10. Participation in any other clinical trials involving investigational or marketed products within 30 days prior to entry in the study.

11. Other conditions that in the opinion of the Principal Investigator(s) may increase risk to the subject and/or compromise the quality of the clinical trial.

12. Concurrent pharmacologic treatment that is required to treat a condition long-term in which concurrent use of dabigatran etexilate is contraindicated.

13. Treatment with any anticoagulant drug for stroke prevention for more than 30 days.

• Aspirin and P2Y12 inhibitors (e.g. clopidogrel (Plavix), or prasugrel (Effient)) are not considered anticoagulant drugs.

• If the subject has received any anticoagulant drug for stroke prevention for less than 30 days, the Principal Investigator(s) or a Co-Investigator will decide whether or not the subject is eligible for this study

14. The Principal Investigator(s) determine(s) that the subject is not eligible for participation in this research study.

Related Conditions & MeSH terms

• Atrial Fibrillation
• Cerebral Ischemic Events
• Cognition Disorders
• Cognitive Dysfunction
• Dementia

Intervention

Drug:
• Dabigatran Etexilate
150 mg BID (CrCL > 30 mL/min) or 75 mg BID (CrCL > 15 to 30 mL/min); Assessment of kidney function every 6 months.
• Warfarin
Dose-adjusted (INR 2.0 - 3.0); Standard warfarin follow-up and education based upon system criteria.

Locations

Country	Name	City	State
United States	Intermountain Heart Institute	Murray	Utah

Sponsors (2)

Lead Sponsor	Collaborator
Intermountain Health Care, Inc.	Boehringer Ingelheim

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incident dementia determined by a formal diagnosis of dementia by a neurologist	Incident dementia will be determined by a formal diagnosis of dementia by a neurologist	24 months
Primary	Moderate decline in cognitive function based on results of the Alzheimer's Disease Assessment Scale and the Disability Assessment for Dementia.	Determined by measuring the change from baseline to study conclusion on the 11-item cognitive subscale of the Alzheimer's Disease Assessment Scale (ADAS-cog11, with scores ranging from 0 to 70, and higher scores indicating greater impairment) and the Disability Assessment for Dementia (DAD, with scores ranging from 0 to 100, and higher scores indicating less impairment). An increase in ADAS-cog11 of >30% is considered significant for moderate cognitive decline. In subjects that score <50% on the DAD, there is a direct correlation with global deterioration scales and scores. Subjects with a 30% decrease in DAD score or those with a score <50% will be considered to have moderate cognitive decline. These scores will be aggregated and if a patient meets either one of the cognitive decline definitions they will be deemed positive for cognitive impairment.	24 months
Secondary	Stroke or Transient ischemic attack (TIA), intracranial bleed		24 months
Secondary	Changes from baseline scores on the mini-mental status evaluation and the Hachinski Ischemic Scale.		24 months