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Botox Injection in Treatment of Cluster Headache

Primary Purpose

Cluster Headache

Status
Completed
Phase
Phase 1
Locations
Norway
Study Type
Interventional
Intervention
Botulinum Toxin Type A 25 IU
Botulinum Toxin Type A 50 IU
Sponsored by
Norwegian University of Science and Technology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cluster Headache focused on measuring Cluster Headache, Botulinum Toxin Type A, Sphenopalatine Ganglion Block, Autonomic Nerve Block

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Informed and written consent
  • Cluster headaches defined in ICHD-2 criteria, duration of periods of attacks normally more than 2 months and insufficient effect of available prophylactic treatment

Exclusion Criteria:

  • Heart or lung disease
  • Any kind of systematic or local disease or illness that may significantly increase the risk of complications for the procedure, related to injection or anesthesia
  • Psychiatric illness that hinders participation in the study
  • Known pregnancy or breast feeding
  • Inadequate use of contraceptives
  • Overuse or abuse of opioids
  • Abuse of medications, narcotics or alcohol
  • Allergy or any other hypersensitivity reactions against marcain, lidocaine, xylocain or adrenalin, botulinum toxin type A, Botox or any of it's constituents or any other related medication
  • Treatment with medication that can interact with botulinum toxin type A

Sites / Locations

  • Department of Neuroscience, Norwegian University of Science and Technology

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Botulinum Toxin Type A 25 IU

Botulinum Toxin Type A 50 IU

Arm Description

The first five patients will be injected 25 IU of Botulinum Toxin Type A

the next five patients will receive 50 IU of Botulinum Toxin Type A

Outcomes

Primary Outcome Measures

Safety aspects / Number of adverse events and number of participants with adverse events as a measure of safety
Number of adverse events and number of participants with adverse events after BTA injection in the area of the sphenopalatine ganglion and severity of adverse events. Registration of any adverse events categorized by probable relationship to drug, the surgical procedure or anesthesia. Data obtained from the headache diaries as well as open questions during consultations.

Secondary Outcome Measures

Cluster headache attack frequency
Hours with cluster headache
Days with cluster headache

Full Information

First Posted
November 21, 2013
Last Updated
March 16, 2017
Sponsor
Norwegian University of Science and Technology
Collaborators
St. Olavs Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02019017
Brief Title
Botox Injection in Treatment of Cluster Headache
Official Title
Endoscopic Block of the Sphenopalatine Ganglion With Botulinum Toxin in Intractable Cluster Headache - Safety Issues
Study Type
Interventional

2. Study Status

Record Verification Date
March 2017
Overall Recruitment Status
Completed
Study Start Date
October 2013 (Actual)
Primary Completion Date
February 2014 (Actual)
Study Completion Date
August 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Norwegian University of Science and Technology
Collaborators
St. Olavs Hospital

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
Cluster headache is an intense and powerful, one-sided headache accompanied by involuntary symptoms such as red eye, droopy eyelids, flow of tears, small pupils and one-sided facial sweating. The headache is believed to be the most intense of all headaches and among many is totally disabling and of great personal and social consequences. For a small group of patients with episodic and most chronic form, drug therapy has little effect. For them, surgery can be a solution. Neuroradiology has found evidence of a possible original activation of cluster headache from the portion of the brain called hypothalamus. Furthermore, an activation of the parasympathetic nervous system through the sphenopalatine ganglion, which may also explain some of the one-sided involuntary symptoms, is suspected in cluster headache. Injection of Botulinum toxin type A (BTA) inhibits secretion of synaptic acetylcholine resulting in nerve signals being blocked. The duration of such a blockade is believed to be 3-9 months. The purpose of the present study is to develop and evaluate a new surgical procedure with injection of BTA for blocking of the sphenopalatine ganglion. The goal is to relieve the symptoms of refractory cluster headache with a minimal invasive procedure. The main objective of the project is to determine the safety of BTA injection in the area of the sphenopalatine ganglion of refractory cluster headache and detect the adverse events. Secondary objectives are to identify the changes of headache attacks by the method used.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cluster Headache
Keywords
Cluster Headache, Botulinum Toxin Type A, Sphenopalatine Ganglion Block, Autonomic Nerve Block

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Botulinum Toxin Type A 25 IU
Arm Type
Experimental
Arm Description
The first five patients will be injected 25 IU of Botulinum Toxin Type A
Arm Title
Botulinum Toxin Type A 50 IU
Arm Type
Experimental
Arm Description
the next five patients will receive 50 IU of Botulinum Toxin Type A
Intervention Type
Drug
Intervention Name(s)
Botulinum Toxin Type A 25 IU
Other Intervention Name(s)
Botox
Intervention Type
Drug
Intervention Name(s)
Botulinum Toxin Type A 50 IU
Other Intervention Name(s)
Botox
Primary Outcome Measure Information:
Title
Safety aspects / Number of adverse events and number of participants with adverse events as a measure of safety
Description
Number of adverse events and number of participants with adverse events after BTA injection in the area of the sphenopalatine ganglion and severity of adverse events. Registration of any adverse events categorized by probable relationship to drug, the surgical procedure or anesthesia. Data obtained from the headache diaries as well as open questions during consultations.
Time Frame
For the follow-up period of 6 months
Secondary Outcome Measure Information:
Title
Cluster headache attack frequency
Time Frame
Average number of attacks of baseline compared to average of week 3 and 4 after injection
Title
Hours with cluster headache
Time Frame
Average of baseline compared to average of week 3 and 4 after injection
Title
Days with cluster headache
Time Frame
Average of baseline compared to average of week 3 and 4 after injection

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: Informed and written consent Cluster headaches defined in ICHD-2 criteria, duration of periods of attacks normally more than 2 months and insufficient effect of available prophylactic treatment Exclusion Criteria: Heart or lung disease Any kind of systematic or local disease or illness that may significantly increase the risk of complications for the procedure, related to injection or anesthesia Psychiatric illness that hinders participation in the study Known pregnancy or breast feeding Inadequate use of contraceptives Overuse or abuse of opioids Abuse of medications, narcotics or alcohol Allergy or any other hypersensitivity reactions against marcain, lidocaine, xylocain or adrenalin, botulinum toxin type A, Botox or any of it's constituents or any other related medication Treatment with medication that can interact with botulinum toxin type A
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniel F Bratbak, MD
Organizational Affiliation
Norwegian University of Science and Technology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Neuroscience, Norwegian University of Science and Technology
City
Trondheim
Country
Norway

12. IPD Sharing Statement

Citations:
PubMed Identifier
26232105
Citation
Bratbak DF, Nordgard S, Stovner LJ, Linde M, Folvik M, Bugten V, Tronvik E. Pilot study of sphenopalatine injection of onabotulinumtoxinA for the treatment of intractable chronic cluster headache. Cephalalgia. 2016 May;36(6):503-9. doi: 10.1177/0333102415597891. Epub 2015 Jul 31.
Results Reference
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Botox Injection in Treatment of Cluster Headache

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