The Effect of Nasal Carbon Dioxide (CO2) in the Treatment of Mild Headache in People Who Experience Migraines
Primary Purpose
Migraine
Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Nasal CO2
Inactive Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Migraine focused on measuring Nasal CO2, Phase II, Adaptive, Randomized, Double-Blind, Placebo-Controlled, Multiple-Dose, Multi-center, Safety, Efficacy, Mild Headache, Migraineur
Eligibility Criteria
Inclusion Criteria:
- Able to read and understand informed consent form and voluntarily consent to participate in this study by signing the IRB-approved informed consent form
- Established diagnosis of migraine with or without aura per ICHD-II (patients with a diagnosis of only menstrual migraine are not eligible)
- History of 2-8 migraine attacks per month during the 3 months prior to randomization
- Have a typical migraine which progresses from a distinct mild headache to a moderate or severe migraine
- Able to recognize a mild headache that could develop into a moderate or severe migraine
Exclusion Criteria:
- Have less than 48 hours of freedom from headache between attacks of migraine
- Have 15 or more headache days per month
- Are females who are pregnant or lactating
- Use antipsychotic or antidepressant medications (unless only for migraine prophylaxis) within 12 weeks prior to randomization and for the duration of the study
- Have a concurrent diagnosis of TMD or trigeminal neuralgia requiring treatment
- Clinically significant deviated septum, nasal polyps or other nasal condition that prevents unrestricted breathing through each nostril
- Have participated in another study with nasal CO2
Sites / Locations
- Capnia Investigative Site
- Capnia Investigative Site
- Capnia Investigative Site
- Capnia Investigative Site
- Capnia Investigative Site
- Capnia Investigative Site
- Capnia Investigative Site
- Capnia Investigative Site
- Capnia Investigative Site
- Capnia Investigative Site
- Capnia Investigative Site
- Capnia Investigative Site
- Capnia Investigative Site
- Capnia Investigative Site
- Capnia Investigative Site
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
1
2
Arm Description
Nasal CO2
Inactive Placebo
Outcomes
Primary Outcome Measures
The proportion of patients who are pain-free
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00690716
Brief Title
The Effect of Nasal Carbon Dioxide (CO2) in the Treatment of Mild Headache in People Who Experience Migraines
Official Title
A Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Safety and Efficacy of Nasal Carbon Dioxide in the Treatment of Mild Headache in Migraineurs
Study Type
Interventional
2. Study Status
Record Verification Date
August 2012
Overall Recruitment Status
Completed
Study Start Date
August 2008 (undefined)
Primary Completion Date
June 2009 (Actual)
Study Completion Date
June 2009 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Capnia, Inc.
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to evaluate the safety and effect of nasal carbon dioxide in the treatment of mild headaches in people who have migraines.
Detailed Description
This multi-center, adaptively randomized, double-blind, placebo-controlled trial will evaluate the efficacy and safety of a nasal, non-inhaled administration of carbon dioxide (CO2) in the treatment of mild headaches. An estimated 250 patients who meet the eligibility criteria will be enrolled into this study at approximately 15 sites to ensure that about 220 patients are randomized and complete the study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Migraine
Keywords
Nasal CO2, Phase II, Adaptive, Randomized, Double-Blind, Placebo-Controlled, Multiple-Dose, Multi-center, Safety, Efficacy, Mild Headache, Migraineur
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
292 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
Nasal CO2
Arm Title
2
Arm Type
Placebo Comparator
Arm Description
Inactive Placebo
Intervention Type
Drug
Intervention Name(s)
Nasal CO2
Intervention Description
Adaptive Randomization to a Dosing Regimen for Treatment of a Qualifying Headache
Intervention Type
Drug
Intervention Name(s)
Inactive Placebo
Intervention Description
Adaptive Randomization to a Dosing Regimen for Treatment of a Qualifying Headache
Primary Outcome Measure Information:
Title
The proportion of patients who are pain-free
Time Frame
2 hours post study drug administration
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Able to read and understand informed consent form and voluntarily consent to participate in this study by signing the IRB-approved informed consent form
Established diagnosis of migraine with or without aura per ICHD-II (patients with a diagnosis of only menstrual migraine are not eligible)
History of 2-8 migraine attacks per month during the 3 months prior to randomization
Have a typical migraine which progresses from a distinct mild headache to a moderate or severe migraine
Able to recognize a mild headache that could develop into a moderate or severe migraine
Exclusion Criteria:
Have less than 48 hours of freedom from headache between attacks of migraine
Have 15 or more headache days per month
Are females who are pregnant or lactating
Use antipsychotic or antidepressant medications (unless only for migraine prophylaxis) within 12 weeks prior to randomization and for the duration of the study
Have a concurrent diagnosis of TMD or trigeminal neuralgia requiring treatment
Clinically significant deviated septum, nasal polyps or other nasal condition that prevents unrestricted breathing through each nostril
Have participated in another study with nasal CO2
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Roger K. Cady, MD
Organizational Affiliation
Clinvest
Official's Role
Study Chair
Facility Information:
Facility Name
Capnia Investigative Site
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35233
Country
United States
Facility Name
Capnia Investigative Site
City
Stanford
State/Province
California
ZIP/Postal Code
94305
Country
United States
Facility Name
Capnia Investigative Site
City
East Hartford
State/Province
Connecticut
ZIP/Postal Code
06118
Country
United States
Facility Name
Capnia Investigative Site
City
West Palm Beach
State/Province
Florida
ZIP/Postal Code
33407
Country
United States
Facility Name
Capnia Investigative Site
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60647
Country
United States
Facility Name
Capnia Investigative Site
City
North Dartmouth
State/Province
Massachusetts
ZIP/Postal Code
02747
Country
United States
Facility Name
Capnia Investigative Site
City
Wellesley Hills
State/Province
Massachusetts
ZIP/Postal Code
02481
Country
United States
Facility Name
Capnia Investigative Site
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48104
Country
United States
Facility Name
Capnia Investigative Site
City
Kalamazoo
State/Province
Michigan
ZIP/Postal Code
49009
Country
United States
Facility Name
Capnia Investigative Site
City
Springfield
State/Province
Missouri
ZIP/Postal Code
65807
Country
United States
Facility Name
Capnia Investigative Site
City
St. Louis
State/Province
Missouri
ZIP/Postal Code
63141
Country
United States
Facility Name
Capnia Investigative Site
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States
Facility Name
Capnia Investigative Site
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States
Facility Name
Capnia Investigative Site
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37203
Country
United States
Facility Name
Capnia Investigative Site
City
Seattle
State/Province
Washington
ZIP/Postal Code
98104
Country
United States
12. IPD Sharing Statement
Learn more about this trial
The Effect of Nasal Carbon Dioxide (CO2) in the Treatment of Mild Headache in People Who Experience Migraines
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