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Transnasal Therapy for Acute Migraine Attack

Primary Purpose

Migraine Disorders

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Humidified oxygen
Dry oxygen
Humidified air
Dry air
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Migraine Disorders focused on measuring Trans-nasal, acute, migraine

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Migraine diagnosis of at least 1 year
  • Migraine attacks between 1 and 15 per month
  • Onset of first migraine < 50 years of age
  • Migraine prophylaxis medication unchanged for 3 months prior to enrollment
  • Meets international classification for headache disorders criteria for diagnosis of episodic migraine with or without aura
  • Able to attend a short treatment session within half hour of onset of headache.

Exclusion Criteria:

  • Known oxygen dependency to maintain arterial oxygen saturation (SaO2) >95%
  • Known marked nasal septal deviation
  • Recurrent epistaxis or chronic Rhino-Sinusitis
  • Concurrent sinus/intranasal surgery
  • Unable to fully understand the consent process and informed consent due to either language barriers or mental capacity.

Sites / Locations

  • Clinical Trials Unit, Johns Hopkins Bayview (JHU ICTR)

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Placebo Comparator

Active Comparator

Arm Label

Humidified oxygen

Dry air

Humidified air

Dry oxygen

Arm Description

Delivering humidified oxygen at 15 liters per minute through the nose and noting the change in primary and secondary outcome variables at 2 hours and 24 hours.

Delivering dry air at 15 liters per minute through the nose and noting the change in primary and secondary outcome variables at 2 hours and 24 hours.

Delivering humidified air at 15 liters per minute through the nose and noting the change in primary and secondary outcome variables at 2 hours and 24 hours.

Delivering dry oxygen at 15 liters per minute through the nose and noting the change in primary and secondary outcome variables at 2 hours and 24 hours.

Outcomes

Primary Outcome Measures

change in pain score as assessed on the VAS scale
Graded on a scale of 1-10 where higher scores mean more pain.

Secondary Outcome Measures

change in nausea score as assessed on the VAS scale
Graded on a scale of 1-10 where higher scores mean more nausea.
change in light sensitivity score as assessed on the VAS scale
Graded on a scale of 1-10 where higher scores mean more light sensitivity.
change in sound sensitivity score as assessed on the VAS scale
Graded on a scale of 1-10 where higher scores mean more sound sensitivity.

Full Information

First Posted
October 15, 2019
Last Updated
July 15, 2020
Sponsor
Johns Hopkins University
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1. Study Identification

Unique Protocol Identification Number
NCT04129567
Brief Title
Transnasal Therapy for Acute Migraine Attack
Official Title
Transnasal Therapy for Acute Migraine Attack
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
August 15, 2018 (Actual)
Primary Completion Date
October 31, 2019 (Actual)
Study Completion Date
November 15, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Migraine is a significant health problem in the United States with 34 million Americans suffering from migraine attacks every year. High-flow oxygen has been successfully used in several clinical studies. Vasoconstriction of blood vessels in the scalp has been proposed as a possible mechanism of action. Some researchers have suggested that the cooling effect of high-flow dry oxygen may be in part responsible for the pain relief. The main objective is to test the hypothesis that the pain relief obtained during high-flow trans-nasal gas therapy is due to the cooling effect of dry gas on the nasal mucosa. The study entails recruiting patients from a headache clinic, being escorted to the Institute for Clinical and Translational Research (ICTR) Johns Hopkins Bayview and randomized into different groups (humidified oxygen, dry air, humidified air and dry oxygen). Eventually, patients will be asked to fill out a questionnaire on pain, nausea, sound and light sensitivity graded on a scale of 1-10. Readings are noted at baseline, 15 mins, 2 hours and 24 hours post-therapy.
Detailed Description
Migraine headaches are associated with significant impairment of quality of life and loss of productivity. High-flow oxygen has been successfully used in several clinical trials and vasoconstriction of blood vessels has been postulated as a possible mechanism. Some researchers have suggested that the cooling effect of high-flow dry oxygen may be in part responsible for the pain relief.The main objective is to test the hypothesis that the pain relief obtained during high-flow intra-nasal gas therapy is due to the cooling effect of dry gas on the nasal mucosa. Participants for this study are recruited from the pool of patients who are already scheduled to attend the headache clinic staffed by the principal investigator. The PI will recruit patients at the Headache Clinic. The patients are escorted to the Clinical Trials Unit (CTU) at the Johns Hopkins Bayview where therapy its provided and will be asked to fill out a questionnaire on pain, nausea, sound and light sensitivity using a visual analog score (VAS) for each symptom on a scale of 1-10. The patients will be randomized to either humidified oxygen, dry air, humidified air or dry oxygen. Patients will be asked to submit readings at the end of therapy, at 2 hours and 24 hours post-therapy. Treatment failure is defined as persistent headache despite treatment with oxygen or air. Participants will be removed from the trial if participants prematurely terminate therapy. The investigators believe that using a total sample size of 45 patients, the investigators will be able to show a statistically significant difference of >2 point change in the VAS pain score reduction between the two treatment groups with a confidence of 80%. No risk were reported in prior studies involving >100 patients and >500 episodes of treatment with air or oxygen. Because of the (at least 2 and 1/2 hour) delay in initiating standard of care treatments, subjects may experience a longer duration and/or intensity of pain from the headache than regular standards of care i.e., sooner. Participants will be reimbursed for participation in this study which will compensate travel and parking.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Migraine Disorders
Keywords
Trans-nasal, acute, migraine

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
51 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Humidified oxygen
Arm Type
Experimental
Arm Description
Delivering humidified oxygen at 15 liters per minute through the nose and noting the change in primary and secondary outcome variables at 2 hours and 24 hours.
Arm Title
Dry air
Arm Type
Experimental
Arm Description
Delivering dry air at 15 liters per minute through the nose and noting the change in primary and secondary outcome variables at 2 hours and 24 hours.
Arm Title
Humidified air
Arm Type
Placebo Comparator
Arm Description
Delivering humidified air at 15 liters per minute through the nose and noting the change in primary and secondary outcome variables at 2 hours and 24 hours.
Arm Title
Dry oxygen
Arm Type
Active Comparator
Arm Description
Delivering dry oxygen at 15 liters per minute through the nose and noting the change in primary and secondary outcome variables at 2 hours and 24 hours.
Intervention Type
Other
Intervention Name(s)
Humidified oxygen
Intervention Description
Delivering humidified oxygen at 15 liters per minute through the nose in a blinded fashion using a nasal cannula.
Intervention Type
Other
Intervention Name(s)
Dry oxygen
Intervention Description
Delivering dry oxygen at 15 liters per minute through the nose in a blinded fashion using a nasal cannula.
Intervention Type
Other
Intervention Name(s)
Humidified air
Intervention Description
Delivering humidified air at 15 liters per minute through the nose in a blinded fashion using a nasal cannula.
Intervention Type
Other
Intervention Name(s)
Dry air
Intervention Description
Delivering dry air at 15 liters per minute through the nose in a blinded fashion using a nasal cannula.
Primary Outcome Measure Information:
Title
change in pain score as assessed on the VAS scale
Description
Graded on a scale of 1-10 where higher scores mean more pain.
Time Frame
2 hours and 24 hours
Secondary Outcome Measure Information:
Title
change in nausea score as assessed on the VAS scale
Description
Graded on a scale of 1-10 where higher scores mean more nausea.
Time Frame
2 hours and 24 hours
Title
change in light sensitivity score as assessed on the VAS scale
Description
Graded on a scale of 1-10 where higher scores mean more light sensitivity.
Time Frame
2 hours and 24 hours
Title
change in sound sensitivity score as assessed on the VAS scale
Description
Graded on a scale of 1-10 where higher scores mean more sound sensitivity.
Time Frame
2 hours and 24 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Migraine diagnosis of at least 1 year Migraine attacks between 1 and 15 per month Onset of first migraine < 50 years of age Migraine prophylaxis medication unchanged for 3 months prior to enrollment Meets international classification for headache disorders criteria for diagnosis of episodic migraine with or without aura Able to attend a short treatment session within half hour of onset of headache. Exclusion Criteria: Known oxygen dependency to maintain arterial oxygen saturation (SaO2) >95% Known marked nasal septal deviation Recurrent epistaxis or chronic Rhino-Sinusitis Concurrent sinus/intranasal surgery Unable to fully understand the consent process and informed consent due to either language barriers or mental capacity.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nauman Tariq, MD
Organizational Affiliation
Johns Hopkins Neurology (Bayview)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clinical Trials Unit, Johns Hopkins Bayview (JHU ICTR)
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21224
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
33631965
Citation
Shah R, Assis F, Narasimhan B, Khachadourian V, Zhou S, Tandri H, Tariq N. Trans-nasal high-flow dehumidified air in acute migraine headaches: A randomized controlled trial. Cephalalgia. 2021 Aug;41(9):968-978. doi: 10.1177/0333102421997766. Epub 2021 Feb 25.
Results Reference
derived

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Transnasal Therapy for Acute Migraine Attack

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