Ticagrelor Therapy for RefrACTORy Migraine Study



Status:Recruiting
Conditions:Migraine Headaches, Migraine Headaches
Therapuetic Areas:Neurology
Healthy:No
Age Range:18 - 65
Updated:4/23/2016
Start Date:October 2015
End Date:September 2017
Contact:Robert J Sommer, MD
Email:rs2463@columbia.edu
Phone:212-342-0886

Use our guide to learn which trials are right for you!

Ticagrelor Therapy for RefrACTORy Migraine Study Pilot (TRACTOR)

This is a prospective, open-label, single-arm pilot study treating 40 subjects to assess the
hypothesis that P2Y, G protein-coupled 12 (P2Y12) inhibition with Brilinta/ticagrelor (90 mg
PO twice a day) reduces episodic and/or chronic migraine headache symptoms in patients with
right to left shunt. Headache frequency while on Brilinta/ticagrelor will be compared with
the documented baseline for each subject. If the Brilinta/ticagrelor therapy was effective
(> 50% reduction in monthly headache days), the subject could elect to continue therapy for
an additional two months (56 days), while continuing to complete daily headache logs.

Migraine headaches are poorly understood, and can be severely debilitating. Many types of
drugs have been tried in migraine sufferers including anti-depressants, anti-seizure
medications, blood pressure medicines and others. The investigators have shown that in a
small number of patients, a certain type of blood thinner (Clopidogrel) can reduce or
eliminate migraine headaches in patients who also have a hole in the heart wall that allows
flow from the right side of the heart to the left. Ticagrelor is a blood thinning drug which
works in the same way as the clopidogrel, but is broken down by the body differently and
thus allows everyone to use it. The investigators wish to test this medication to see if it
works as well, or better than the clopidogrel.

Inclusion Criteria:

- At least one year history of Episodic or Chronic migraine headache symptoms

- At least 6 headache days per month

- Subject able to complete online daily headache log

Exclusion Criteria:

- Inability to understand the study or history of non-compliance with medical advice

- Currently taking a P2Y12 inhibitor

- Known hypersensitivity to Brilinta/ticagrelor

- History of stroke/transient ischemic attack (TIA) in the previous 6 months

- Active bleeding from any site

- Active peptic ulcer disease or upper gastrointestinal (GI) bleeding within six (6)
months

- Migraine onset after 50 years of age

- Renal impairment: Creatinine Clearance < 60 cc/min

- Severe hepatic impairment with total bilirubin > 3.0 mg/dL

- Thrombocytopenia with platelet count < 100,000 / ul

- History of intracranial hemorrhage

- Contraindications to blood thinner therapy or history of major bleeding episode while
taking blood thinner therapy

- Need for chronic oral anti-coagulation therapy (i.e. Atrial Fibrillation)

- Need for chronic anti-platelet therapy (i.e. drug-eluting (DE) Stent), including
daily aspirin use

- Need for daily nonsteroidal anti-inflammatory drug (NSAID) use

- Need for daily carbamazepine therapy or other strong CYP3A inhibitors or potent CYP3A
inducers

- Need for simvastatin or lovastatin greater than 40 mg daily

- Symptomatic bradycardia or syncope

- Pregnancy or currently breast-feeding, or plan to become pregnant during the study
period

- Planned surgery during the study time-frame

- Previously implanted patent foramen ovale (PFO), atrial septal defect (ASD),
pacemaker, inferior vena cava filter, or left atrial appendage closure device
We found this trial at
1
site
630 W 168th St
New York, New York
212-305-2862
Principal Investigator: Robert Sommer, MD
Phone: 347-514-3366
Columbia University Medical Center Situated on a 20-acre campus in Northern Manhattan and accounting for...
?
mi
from
New York, NY
Click here to add this to my saved trials