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Intranasal Cooling for Cluster Headache and Migraine (COOLHEAD)

Primary Purpose

Migraine, Cluster Headache

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
RhinoChill intranasal cooling
Sponsored by
Cumbria Partnership NHS Foundation Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Migraine focused on measuring Migraine, Cluster headache, headache

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • >18 Years old.
  • Meets criteria for NICE guidelines diagnosis of cluster headache or chronic migraine
  • Has not responded satisfactorily to migraine prophylaxis or standard analgesia
  • Capable of giving informed consent

Exclusion Criteria:

  • < 18 years of age
  • Subject has history of other severe co-morbid illness which would prevent full participation in the study
  • Inability to insert the nasal cannulae
  • Known temperature sensitive disorder such as reynauds, cryoglobulinaemia
  • Known oxygen dependency to maintain SaO2 >95%

Sites / Locations

  • Neurosciences department, Penrith Hospital, Cumbria Partnership NHS Foundation Trust

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Intranasal Cooling

Arm Description

RhinoChill Intranasal cooling, administered for 20 minutes. 10 treatment sessions per participant.

Outcomes

Primary Outcome Measures

• Reduction of pain score and overall symptoms from baseline in Migraine/cluster headache sufferers
When a participant presents with headache, baseline assessments will be performed for pain, nausea and other recognised symptoms of migraine/cluster headache. The Rhinochill device will be used to provide transnasal cooling for a period of 20 minutes then reassessment of pain and other symptoms will be undertaken.

Secondary Outcome Measures

Tolerance to Rhinochill cooling during maximum 20 minutes treatment
Visual/analogue pain score and visual/analogue discomfort score
Adverse events noted throughout treatment phase and during follow up
• Any adverse events noted during the treatment or following treatment and during routine follow up will be recorded and analysed.

Full Information

First Posted
July 10, 2013
Last Updated
December 3, 2014
Sponsor
Cumbria Partnership NHS Foundation Trust
Collaborators
BeneChill, Inc
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1. Study Identification

Unique Protocol Identification Number
NCT01898455
Brief Title
Intranasal Cooling for Cluster Headache and Migraine
Acronym
COOLHEAD
Official Title
IntraNasal Evaporative Cooling for the Symptomatic Relief of Migraine and Cluster Headache
Study Type
Interventional

2. Study Status

Record Verification Date
December 2014
Overall Recruitment Status
Completed
Study Start Date
August 2013 (undefined)
Primary Completion Date
August 2014 (Actual)
Study Completion Date
August 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Cumbria Partnership NHS Foundation Trust
Collaborators
BeneChill, Inc

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will be looking at the clinical efficacy of using a intranasal evaporative cooling device in providing relief of the symptoms of migraine and cluster headache. It will involve using a nasal catheter to spray a liquid coolant into the nasal cavity where it evaporates and removes heat from the tissue, thereby cooling the tissue and the blood vessels which supply blood to the brain. This cooling effect will cause the blood vessels to constrict and it is thought that this may provide symptomatic relief in both these forms of headache. 10 migraine patients and 5 cluster headache patients will be enrolled in the study and will receive 10 treatments each, for a maximum of 20 minutes at a time. They will be monitored during the treatment and for two hours afterwards to assess headache severity and side effects. There will be a further follow up 2 months after the last treatment to assess for longer term side effects from the treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Migraine, Cluster Headache
Keywords
Migraine, Cluster headache, headache

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intranasal Cooling
Arm Type
Experimental
Arm Description
RhinoChill Intranasal cooling, administered for 20 minutes. 10 treatment sessions per participant.
Intervention Type
Device
Intervention Name(s)
RhinoChill intranasal cooling
Other Intervention Name(s)
RhinoChill, Intranasal cooling, transnasal cooling
Intervention Description
The RhinoChill device will be used to locally cool the posterior nasopharynx, surrounding tissues and vasculature using a variable cooling flow rate based on patient comfort and tolerance, for a maximum of 20 minutes. Local anaesthetic spray will be administered to patients if the nasal catheters or cooling is poorly tolerated.
Primary Outcome Measure Information:
Title
• Reduction of pain score and overall symptoms from baseline in Migraine/cluster headache sufferers
Description
When a participant presents with headache, baseline assessments will be performed for pain, nausea and other recognised symptoms of migraine/cluster headache. The Rhinochill device will be used to provide transnasal cooling for a period of 20 minutes then reassessment of pain and other symptoms will be undertaken.
Time Frame
20 minutes
Secondary Outcome Measure Information:
Title
Tolerance to Rhinochill cooling during maximum 20 minutes treatment
Description
Visual/analogue pain score and visual/analogue discomfort score
Time Frame
20 minutes
Title
Adverse events noted throughout treatment phase and during follow up
Description
• Any adverse events noted during the treatment or following treatment and during routine follow up will be recorded and analysed.
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: >18 Years old. Meets criteria for NICE guidelines diagnosis of cluster headache or chronic migraine Has not responded satisfactorily to migraine prophylaxis or standard analgesia Capable of giving informed consent Exclusion Criteria: < 18 years of age Subject has history of other severe co-morbid illness which would prevent full participation in the study Inability to insert the nasal cannulae Known temperature sensitive disorder such as reynauds, cryoglobulinaemia Known oxygen dependency to maintain SaO2 >95%
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jitka Vanderpol, MD
Organizational Affiliation
Cumbria Partnership NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Neurosciences department, Penrith Hospital, Cumbria Partnership NHS Foundation Trust
City
Penrith
State/Province
Cumbria
ZIP/Postal Code
CA11 8HX
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
25623151
Citation
Vanderpol J, Bishop B, Matharu M, Glencorse M. Therapeutic effect of intranasal evaporative cooling in patients with migraine: a pilot study. J Headache Pain. 2015 Jan 26;16:5. doi: 10.1186/1129-2377-16-5.
Results Reference
derived

Learn more about this trial

Intranasal Cooling for Cluster Headache and Migraine

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