View Clinical Trial (Medical Research Study)
A Double-blind, Placebo-controlled Pilot Study to Collect and Evaluate Data on the Use of Intravenous Ibuprofen in the Treatment of an Acute Migraine
| City: |
|
Philadelphia |
| State: |
|
Pennsylvania |
| Zip Code: |
|
19107 |
| Conditions: |
|
Episodic Migraine |
| Purpose: |
|
This is a pilot trial to collect and evaluate data on the use of intravenous ibuprofen
(IVIb) in the treatment of an acute migraine attack. Data will be collected on the efficacy
of IVIb in subjects who are treated with study medication between 2 and 72 hours from time
of onset of headache.
Periodic safety and efficacy assessments will be performed prior to and after study drug
administration.
Null hypothesis: There is no difference in the proportion of subjects in the 2 treatment
groups (active treatment and placebo) who have pain relief at 2 hours after the completion
of the double-blind treatment infusion. Pain relief is defined as a reduction in headache
pain level from severe or moderate decreased to mild or headache-free, respectively.
|
| Study Summary: |
|
|
| Criteria: |
|
Inclusion Criteria:
- Male and female subjects between the ages of 18 and 65, inclusive
- Subject diagnosed with episodic migraine, with or without aura according to ICHD-2
criteria for at least one-year prior to screening
- Subject experiences between 2-10 migraine attacks per month (during the previous 6
months) with no more than 15 days of headache per month.
- Subject is using or agrees to use for the duration of participation a medically
acceptable form of contraception (as determined by investigator), if female and of
child-bearing potential
- Subject is able to come for 4 hour in-clinic treatment of an acute migraine attack
- Subjects are able to understand and comply with all study procedures.
- Subject provides written informed consent prior to any screening procedures being
conducted
- If subject is on an allowable migraine preventive medication, the dose has been
stable for at least 4 weeks prior to screening and the dose will remain stable
throughout study participation.
Exclusion Criteria:
- Unable to make a reliable self-report of pain intensity to pain relief
- Use of analgesic or opioid within 24 hours of onset of headache to be treated with
study medication. (If subject has an eligible headache and has taken a triptan or
DHE within 24 hours, but greater than 2 hours before study drug dosing, they can be
treated with study medication.)
- Patients taking the following medications on a regular basis: warfarin, lithium,
ACE-inhibitors, loop diuretics, thiazide diuretics, ARBs, and methotrexate.
- Patients with active, clinically significant anemia
- Patients with a history or evidence of asthma
- Patients with a history heart failure
- Subjects with severely impaired hepatic or renal function, as determined by the
investigator
- Patients with a history of allergy or hypersensitivity to any component of IVIb,
aspirin (or aspirin related products), NSAIDs, or COX-2 inhibitors
- Pregnant or nursing women
- Patients who have a history of congenital bleeding diathesis (e.g., hemophilia) or
any active clinically significant bleeding, or have underlying platelet dysfunction
including (but not limited to) idiopathic thrombocytopenic purpura, disseminated
intravascular coagulation, or congenital platelet dysfunction
- Patients who have GI bleeding that required medical intervention within the previous
6 weeks (unless definitive surgery has been performed.)
- Patients who have a platelet count less than 100,000, as determined within the 28
days prior to treatment
- Pre-existing or current dependence on opioids.
- Subjects who have participated in an investigational drug trial in the 30 days prior
to the screening visit
- Subjects with uncontrolled hypertension
|
| NCT ID: |
|
NCT01230411 |
| Primary Contact: |
|
Principal Investigator
Stephen D. Silberstein, M.D.
Jefferson Headache Center
Meryl Latsko, MD,MPH
Phone: 215-955-9477
Email: meryl.latsko@jefferson.edu
|
| Backup Contact: |
|
Email: kathleen.bradlely@jefferson.edu
Kathleen Bradley, BSN, CCRP
Phone: 215-955-2025
|
| Location Contact: |
|
Philadelphia, Pennsylvania 19107
United States
Kathleen Bradley, BSN
Email: kathleen.bradley@jefferson.edu
Site Status: Recruiting |
| Data Source: |
|
ClinicalTrials.gov |
| Date Processed: |
|
June 18, 2013 |
| Modifications to this listing: |
|
Only selected fields are shown, please use the link
below to view all information about this clinical trial. |
|
Click to view Full Listing
|