Abobotulinumtoxina Efficacy in Post-Traumatic Headache
Primary Purpose
Post-Traumatic Headache
Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
AbobotulinumtoxinA
Normal saline
Sponsored by
About this trial
This is an interventional treatment trial for Post-Traumatic Headache
Eligibility Criteria
Inclusion Criteria:
- male or female
- age 18-65
- meets International Classification Headache Disorders II (ICHD-II) criteria for post-traumatic headache
- average pain score of greater than 4/10 in severity on the numerical rating system
- Rancho Los Amigos cognitive scale score greater than seven.
Exclusion Criteria:
- Uncontrolled medical condition other than PTH
- Severe additional chronic pain complaint which could not be distinguished from headache pain
- pregnancy, breast feeding,
- prior treatment with botulinum toxin within one year of enrollment
- current substance abuse/dependence
- medical condition that would increase risk of neuromuscular junction blockade with botulinum toxin (myasthenia gravis, Eaton Lambert, amyotrophic lateral sclerosis)
- poorly controlled psychiatric
- initiation of a new anti-depressant or anti-seizure medication within three months of enrolling in study
- ongoing disability or litigation claim.
Sites / Locations
- VA Greater Los Angeles Healthcare System
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Abobotulinumtoxina
Placebo
Arm Description
300 units of abobotulinumtoxinA was reconstituted with 2.4 ml of 0.9% preservative free sterile saline so that each 0.1 ml contained 12.5 units of Abobotulinumtoxina 0.1 ml were injected into 31 sites of the head and neck
0.9% preservative free sterile saline. 0.1 ml were injected into 31 sites of the head and neck
Outcomes
Primary Outcome Measures
Incidence of headaches from baseline
Evaluation in weekly incidence of headaches from baseline based on headache diary or weekly phone follow-up
Secondary Outcome Measures
Intensity of headache pain
Evaluation of pain intensity using score of headache on Numerical Rating Scale (NRS) over time. The NRS is an 11-point scale for patient self-reporting of pain with 0 being no pain and 10 being the most severe pain.
Number of headache days per week
Evaluation of the number of days a headache was present over each week
Full Information
NCT ID
NCT03928496
First Posted
April 18, 2019
Last Updated
April 24, 2019
Sponsor
VA Greater Los Angeles Healthcare System
Collaborators
Ipsen
1. Study Identification
Unique Protocol Identification Number
NCT03928496
Brief Title
Abobotulinumtoxina Efficacy in Post-Traumatic Headache
Official Title
Abobotulinumtoxina Efficacy in Post-Traumatic Headache
Study Type
Interventional
2. Study Status
Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
August 1, 2013 (Actual)
Primary Completion Date
February 2, 2017 (Actual)
Study Completion Date
February 2, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Greater Los Angeles Healthcare System
Collaborators
Ipsen
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study will evaluate the efficacy of abobotulinumtoxina on Veterans with post-traumatic headache
Detailed Description
A significant proportion of headaches occur following head trauma, and therefore are referred to as post-traumatic headaches (PTH). Traumatic brain injury (TBI) is highly prevalent in the Operation Iraqi Freedom/Operation Enduring Freedom (OIF/OEF) population and consequently there has been a rise in PTH in the clinical setting at VA hospitals. Botulinum toxin type A (BoNT-A) has been shown to be effective in treating chronic migraine and chronic daily headache. It is therefore reasonable to predict that BoNT-A may also be effective in treating PTH. This study proposes that PTH and its associated symptoms may respond positively to BoNT-A treatment due to its similar pathophysiology and clinical resemblance to other headache disorders including tension type headache, typical migraine with or without aura, and chronic daily headache.
Study Design: Veterans with mild, moderate or severe brain injury with a headache developing within 7 days after head trauma and persisting greater than 3 months were recruited from the Veterans Affairs Greater Los Angeles Healthcare System. The study is a prospective, double-blind, randomized, placebo-controlled, cross-over trial.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post-Traumatic Headache
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Masking Description
The project statistician used a computer-based random number generator to create a randomized treatment allocation schedule that was provided to the pharmacist and nurse practitioner who did not disclose this information. The pharmacist provided the nurse practitioner with the medication in an unlabeled bag, which either included BoNT-A or Normal Saline. Patients were randomized to receive BoNT-A or Normal Saline as first injection. The nurse practitioner reconstituted the medication in a separate room and then provided the investigator with unlabeled syringes.
Allocation
Randomized
Enrollment
40 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Abobotulinumtoxina
Arm Type
Experimental
Arm Description
300 units of abobotulinumtoxinA was reconstituted with 2.4 ml of 0.9% preservative free sterile saline so that each 0.1 ml contained 12.5 units of Abobotulinumtoxina 0.1 ml were injected into 31 sites of the head and neck
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
0.9% preservative free sterile saline. 0.1 ml were injected into 31 sites of the head and neck
Intervention Type
Drug
Intervention Name(s)
AbobotulinumtoxinA
Other Intervention Name(s)
Dysport
Intervention Description
Subjects were injected with 0.1 ml (12.5 units of Abobotulinumtoxina) into 31 distinct muscle locations in the head and neck
Intervention Type
Drug
Intervention Name(s)
Normal saline
Intervention Description
Subjects were injected with 0.1 ml of preservative free normal saline into 31 distinct muscle locations in the head and neck
Primary Outcome Measure Information:
Title
Incidence of headaches from baseline
Description
Evaluation in weekly incidence of headaches from baseline based on headache diary or weekly phone follow-up
Time Frame
evaluation from time of injection until completion of 12 week follow-up
Secondary Outcome Measure Information:
Title
Intensity of headache pain
Description
Evaluation of pain intensity using score of headache on Numerical Rating Scale (NRS) over time. The NRS is an 11-point scale for patient self-reporting of pain with 0 being no pain and 10 being the most severe pain.
Time Frame
evaluation from time of injection until completion of 12 week follow-up
Title
Number of headache days per week
Description
Evaluation of the number of days a headache was present over each week
Time Frame
evaluation from time of injection until completion of 12 week follow-up
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
male or female
age 18-65
meets International Classification Headache Disorders II (ICHD-II) criteria for post-traumatic headache
average pain score of greater than 4/10 in severity on the numerical rating system
Rancho Los Amigos cognitive scale score greater than seven.
Exclusion Criteria:
Uncontrolled medical condition other than PTH
Severe additional chronic pain complaint which could not be distinguished from headache pain
pregnancy, breast feeding,
prior treatment with botulinum toxin within one year of enrollment
current substance abuse/dependence
medical condition that would increase risk of neuromuscular junction blockade with botulinum toxin (myasthenia gravis, Eaton Lambert, amyotrophic lateral sclerosis)
poorly controlled psychiatric
initiation of a new anti-depressant or anti-seizure medication within three months of enrolling in study
ongoing disability or litigation claim.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Milena Zirovich, MD
Organizational Affiliation
VA Greater Los Angeles
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA Greater Los Angeles Healthcare System
City
Los Angeles
State/Province
California
ZIP/Postal Code
90073
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
A de-identified dataset may be provided upon request
IPD Sharing Time Frame
Starting at 3 months following publication and up to 3 years after publication
IPD Sharing Access Criteria
Data access requests will be reviewed and requestors will sign a data access agreement
Learn more about this trial
Abobotulinumtoxina Efficacy in Post-Traumatic Headache
We'll reach out to this number within 24 hrs