A Pilot Study on Edoxaban for the Resolution of Left Atrial Thrombosis in Patients With Non-valvular Atrial Fibrillation

Atrial Fibrillation Clinical Trial

Official title:

A Pilot Study on Edoxaban for the Resolution of Left Atrial Thrombosis in Patients With Non-valvular Atrial Fibrillation

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03489395
• Other study ID #: EDO-SP-01-2015
• Secondary ID: 2015-004847-37
• Status: Completed
• Phase: Phase 2
• Start date: January 30, 2018
• Est. completion date: April 30, 2021

Study information

• Verified date: May 2021
• Source: G. d'Annunzio University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Isolated reports have indicated that complete Left Atrial or Left Atrial Appendage thrombus resolution may be achieved also with use of oral Factor Xa inhibitors, which have demonstrated the same efficacy but a better safety profile compared to warfarin.

The aim of this open-label pilot study is to investigate the percentage of Left Atrial /Left Atrial Appendage thrombus resolution with edoxaban therapy in patients with non-valvular atrial fibrillation. The subordinated aim is the design a larger and longer study to compare edoxaban and warfarin in the same patient population.

With the exception of few case reports, there are no data in the same patient population referred to antithrombotic treatments other than vitamin K antagonists.

Description:

This is a non-controlled, open-label, 4 weeks pilot study.

As the main goal of this exploratory study is the estimation of the magnitude of the Left Atrial /Left Atrial Appendage thrombus resolution with edoxaban, no control group with vitamin K antagonists has been considered, providing that, for the purpose of this study, the magnitude of the response of warfarin is satisfactory defined.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 25
• Est. completion date: April 30, 2021
• Est. primary completion date: December 31, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 99 Years

Eligibility

Inclusion Criteria:

Patients with all the following criteria will be eligible for inclusion in the study protocol:

1. Signed written informed consent.

2. Males and females = 18 years of age.

3. Female subjects must be post-menopausal (for at least 2 years), surgically sterile, abstinent, or, if sexually active, be practicing an effective method of birth control (e.g., prescription oral contraceptives, contraceptive injections, intrauterine device, double-barrier method, contraceptive patch, male partner sterilization) before entry and throughout the study; and, for those of childbearing potential, have a negative serum ß-human chorionic gonadotropin pregnancy test at screening.

4. Atrial fibrillation (AF) must be documented by ECG evidence (e.g., 12-lead ECG, rhythm strip, Holter, pacemaker interrogation) within 30 days before enrolment.

5. Subjects with newly diagnosed atrial fibrillation are eligible provided that:

• -there is evidence that the atrial fibrillation is non-valvular:

• -there is ECG evidence on 2 occasions 24 hours apart demonstrating atrial fibrillation.

6. Left Atrial or Left Atrial Appendage thrombosis documented by trans-esophageal echocardiography (TEE)

7. Cardiac failure, Hypertension, Age (x2 ), Diabetes, Stroke (x 2) risk index-VASC score >1.

Exclusion Criteria:

Patients with all the following criteria will not be eligible for inclusion in the study protocol:

1. Hemodynamically significant mitral valve stenosis.

2. Prosthetic heart mechanical or biological valve (annuloplasty with or without prosthetic ring, commissurotomy and/or valvuloplasty are permitted).

3. Transient atrial fibrillation caused by a reversible disorder (e.g., thyrotoxicosis, pulmonary embolism, recent surgery or myocardial infarction).

4. Known presence of atrial myxoma.

5. Left ventricular thrombus.

6. Active endocarditis.

7. Active internal bleeding.

8. History of condition associated with increased bleeding risk including, but not limited to:

• major surgical procedure or trauma within 30 days;

• clinically significant gastrointestinal bleeding within 6 months;

• previous intracranial, intraocular, spinal, atraumatic intra-articular bleeding;

• chronic haemorrhagic disorder;

• Any neoplasm, including intracranial neoplasm,

• arteriovenous malformation or aneurysm.

9. Platelet count <90,000/µL at the screening visit.

10. Sustained uncontrolled hypertension: Systolic Blood Pressure =180 mmHg or Diastolic Blood Pressure =100 mmHg.

11. Severe, disabling stroke (modified Rankin score of 4 to 5, inclusive within 3 months or any stroke < 14 days).

12. Transient ischemic attack within 3 days.

13. Any oral anticoagulant therapy at the time of the baseline visit.

14. Treatment with:

• aspirin >160 mg daily;

• aspirin plus a thienopyridine within 5 days;

• intravenous antiplatelets within 5 days;

• fibrinolytics within 10 days.

15. Anticipated need for therapy with a non-steroidal anti-inflammatory drug in the next 4 weeks.

16. Treatment with a strong inducer of cytochrome P450 and P glycoprotein, such as ketoconazole, itraconazole, voriconazole, posaconazole, ritonavir, lopinavir, telaprevir, indinavir, conivaptan, clarithromycin or planned treatment during the study.

17. Other indication for anticoagulant therapy.

18. Hypersensitivity or intolerance to the study drug, including excipients.

19. Women of childbearing potential who do not want adopt a contraceptive method during the study period and the following 4 weeks.

20. Breast-feeding women during the study period and the following 4 weeks.

21. Anemia (hemoglobin <10 g/dL) at the screening visit.

22. Known significant liver disease (e.g., acute clinical hepatitis, chronic active hepatitis, cirrhosis), or Alanine aminotransferase or Aspartate aminotransferase >2 x Upper Level of Normal or total bilirubin >1.5 x Upper Level of Normal.

23. Patients with moderate or severe renal impairment (CrCL <50 mL/min) or patients with end stage renal disease (CrCL < 15 mL/min) or on dialysis.

Related Conditions & MeSH terms

• Atrial Fibrillation
• Thrombosis

Intervention

Drug:
• Edoxaban
Edoxaban 60 mg once a day for 4 weeks. Edoxaban 30 mg/day in patients with body weight =60 kg, or with concomitant therapy with verapamil/quinidine/dronedarone.

Locations

Country	Name	City	State
Italy	Ospedale generale regionale "F. Miulli"	Acquaviva delle Fonti	Bari
Italy	AORN S.ANNA e S.SEBASTIANO	Caserta
Italy	Università degli Studi G. D'Annunzio	Chieti
Italy	Ospedale P. Monaldi	Napoli
Italy	Policlinico AO di Padova	Padova
Italy	Presidio Ospedaliero S. Maria delle Grazie	Pozzuoli	Napoli
Italy	Policlinico Universitario Campus Bio-Medico	Roma
Italy	Ospedale Madonna del Soccorso	San Benedetto Del Tronto	Ascoli Piceno

Sponsors (2)

Lead Sponsor	Collaborator
Raffaele De Caterina	Hippocrates Research

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Safety analysis - Percentage of bleeding events (telephone assessment)	Only a descriptive statistical analysis will be performed.	4 weeks and 8 weeks
Other	Safety analysis - Percentage of any stroke or peripheral embolism (telephone assessment)	Only a descriptive statistical analysis will be performed.	4 weeks and 8 weeks
Other	Safety analysis - Percentage of any other safety related events (deaths, Serious Adverse Events and Adverse Events).	Only a descriptive statistical analysis will be performed.	4 weeks and 8 weeks
Primary	Percentage of patients with complete thrombus resolution by TEE, evaluated with the following Probe angulations: 0°, 45°-to-60°, 90°.	Only a descriptive statistical analysis will be performed.	4 weeks
Secondary	Absolute variation of thrombus area by TEE evaluation (Probe angulations: 0°, 45-to-60°, 90°)	Only a descriptive statistical analysis will be performed.	4 weeks
Secondary	Percent variation of thrombus area by TEE evaluation (Probe angulations: 0°, 45-to-60°, 90°)	Only a descriptive statistical analysis will be performed.	4 weeks
Secondary	Time to electrical cardioversion (when applicable).	Only a descriptive statistical analysis will be performed.	4 weeks