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Evaluation of Efficacy and Safety of add-on Alpha-lipoic Acid on Migraine Prophylaxis in Adolescent Population

Primary Purpose

Adolescent Migraine

Status
Completed
Phase
Phase 4
Locations
India
Study Type
Interventional
Intervention
Flunarizine 5mg
Alpha lipoic acid 300mg
Sponsored by
All India Institute of Medical Sciences, Bhubaneswar
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Adolescent Migraine focused on measuring Adolescent Migraine, Flunarizine, Alpha Lipoic Acid, Thiol Level, Calcitonin gene regulated peptide

Eligibility Criteria

10 Years - 19 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with "15 or more headache days per month with at least 8 days having migraine features for at least 3 months (according to the criteria of the International Classification of Headache Disorders, 3rd edition [beta version], or ICHD-3 beta)."
  • Adolescent migraineurs aged 10 to 19 years of age of either sex.
  • Patients who have not taken any prophylactic treatment within the last three months before their inclusion in the study.
  • Patients and/or parents have given informed written consent/assent.

Exclusion Criteria:

  • Patient with headache other than migraine.
  • Patients who were on corticosteroids
  • Treatment with any test drugs in the preceding three months from the start of the trial.
  • If there is any history of interventions or devices used for the treatment of migraine, such as transcranial magnetic stimulation and nerve blocks during the 3 months before screening.
  • Any other accompanying systemic illness; abnormalities revealed on neurologic examination.
  • Psychiatric disturbances, history of epilepsy , learning disabilities, head trauma or use of other drugs acting on the central nervous system, including, smoking, alcohol consumption or any illicit drug abuse

Sites / Locations

  • AIIMS

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Flunarizine

Alpha Lipoic Acid

Arm Description

flunarizine will be prescribed at a dose of 5mg once daily , orally for 12 weeks

Alpha Lipoic Acid will be prescribed at a dose of 300mg once daily,orally for 12 weeks

Outcomes

Primary Outcome Measures

Mean monthly migraine attack rate
Change in the mean monthly migraine attack rate from baseline after treatment with Flunarizine vs Alpha Lipoic Acid

Secondary Outcome Measures

Responder rate
percentage of patients having ≥50% reduction in migraine frequency from baseline after treatment with Flunarizine vs Alpha Lipoic Acid
The number of days with migraine headache
The number of days with migraine headache from baseline after treatment with Flunarizine vs Alpha Lipoic Acid
The mean severity of acute attacks
The mean severity of acute attacks will be considered as severity basis where 3 will be severe and 1 will be mild attack (on a 3-point scale: 3, severe; 2, moderate; 1, mild) from baseline after treatment with Flunarizine vs Alpha Lipoic Acid
The number of days with nausea or vomiting
The number of days with nausea or vomiting from baseline after treatment with Flunarizine vs Alpha Lipoic Acid
The headache disability will be assessed by pedMIDAS (pediatric migraine disability assessment score)
The headache disability will be assessed by pedMIDAS (pediatric migraine disability assessment score) scoring system (denotes 0 to 10 as little to no dyability and greater than 50 as severe disability) from baseline after treatment with Flunarizine vs Alpha Lipoic Acid
The relapse rate among the responders after stoppage of prophylactic therapy .
The relapse rate among the responders after stoppage of prophylactic therapy over the next 12 weeks.
Serum thiol levels
Serum thiol levels from baseline after treatment with Flunarizine vs Alpha Lipoic Acid
Serum CGRP
Serum CGRPlevels from baseline after treatment with Flunarizine vs Alpha Lipoic Acid

Full Information

First Posted
August 20, 2019
Last Updated
July 24, 2023
Sponsor
All India Institute of Medical Sciences, Bhubaneswar
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1. Study Identification

Unique Protocol Identification Number
NCT04064814
Brief Title
Evaluation of Efficacy and Safety of add-on Alpha-lipoic Acid on Migraine Prophylaxis in Adolescent Population
Official Title
Evaluation of Efficacy and Safety of add-on Alpha-lipoic Acid on Migraine Prophylaxis in Adolescent Population: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Completed
Study Start Date
September 14, 2019 (Actual)
Primary Completion Date
April 30, 2021 (Actual)
Study Completion Date
June 30, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
All India Institute of Medical Sciences, Bhubaneswar

4. Oversight

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

5. Study Description

Brief Summary
Migraine causes a substantial impact on the physical and mental health of a child and it is a major cause for time-off school leading to impaired academic performance. Therefore prophylactic treatment is suggested for adolescents with frequent or disabling migraine, aiming at improving the function, quality of life and reducing disability. The most commonly used non-pharmacological agents for the prophylactic management of migraine in adolescents are nutraceuticals. Amongst all nutraceuticals, most commonly used agents for prophylaxis are coenzyme Q10, magnesium, riboflavin, feverfew and butterbur . Alpha-lipoic acid (ALA) or 6,8-thioctic acid, is an endogenous molecule which functions as an important co-factor for various enzyme complexes in mitochondria and plays an important role in energy metabolism.ALA is a nutraceutical agent which also has neuroprotective and anti-inflammatory effects. It has been proved that the thiol level remains low in migraine patients. However, only one study has been done by Ali et al in the pediatric population where the combination of ALA and topiramate has shown promising results but the study result is not generalizable due to its inherent limitations. So, the study has been planned with an aim to evaluate the efficacy and safety of ALA as add-on therapy with flunarizine in the adolescent age group
Detailed Description
Migraine causes a substantial impact on the physical and mental health of a child and it is a major cause for time-off school leading to impaired academic performance. Therefore prophylactic treatment is suggested for adolescents with frequent or disabling migraine, aiming at improving the function, quality of life and reducing disability. Pharmacological agents commonly used for migraine prophylaxis in adolescents are topiramate, cyproheptadine, amitriptyline, valproate, propranolol and flunarizine. These preventive medications are effective first-line treatment but the associated adverse effects have limited their use amongst the adolescent population. In this clinical scenario nutraceuticals may be an alternative option. The most commonly used non-pharmacological agents for the prophylactic management of migraine in adolescents are nutraceuticals. Amongst all nutraceuticals, most commonly used agents for prophylaxis are coenzyme Q10, magnesium, riboflavin, feverfew and butterbur . Despite being largely used for prophylaxis of adolescent migraine, sufficient evidences are lacking which support the safety and efficacy of these agents. The findings from the previous studies on riboflavin and coenzyme Q10 are conflicting and inconclusive. Thus there is a need for a clinically effective nutraceutical in migraine prophylaxis. Alpha-lipoic acid (ALA) or 6,8-thioctic acid, is an endogenous molecule which functions as an important co-factor for various enzyme complexes in mitochondria and plays an important role in energy metabolism. ALA is a nutraceutical agent which also has neuroprotective and anti-inflammatory effects. It has been proved that the thiol level remains low in migraine patients. In some recent studies, ALA has been found to be beneficial in migraine prophylaxis in adults. However, only one study has been done by Ali et al in the pediatric population where the combination of ALA and topiramate has shown promising results but the study result is not generalizable due to its inherent limitations. From the literature search, it is evident that there is a lack of data on the efficacy and safety of ALA as a prophylactic agent in migraine. So, the study has been planned with an aim to evaluate the efficacy and safety of ALA as add-on therapy with flunarizine in the adolescent age group. The choice of flunarizine as standard prophylactic therapy in the present study is supported by the fact that flunarizine is efficacious and safer in the adolescent population due to its fewer adverse effects in comparison to topiramate and propranolol.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adolescent Migraine
Keywords
Adolescent Migraine, Flunarizine, Alpha Lipoic Acid, Thiol Level, Calcitonin gene regulated peptide

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Randomized, open Label , active controlled study
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Flunarizine
Arm Type
Active Comparator
Arm Description
flunarizine will be prescribed at a dose of 5mg once daily , orally for 12 weeks
Arm Title
Alpha Lipoic Acid
Arm Type
Experimental
Arm Description
Alpha Lipoic Acid will be prescribed at a dose of 300mg once daily,orally for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Flunarizine 5mg
Intervention Description
Flunarizine 5mg once daily,orally for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Alpha lipoic acid 300mg
Intervention Description
Alpha lipoic acid 300mg ,once daily ,orally for 12 weeks
Primary Outcome Measure Information:
Title
Mean monthly migraine attack rate
Description
Change in the mean monthly migraine attack rate from baseline after treatment with Flunarizine vs Alpha Lipoic Acid
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Responder rate
Description
percentage of patients having ≥50% reduction in migraine frequency from baseline after treatment with Flunarizine vs Alpha Lipoic Acid
Time Frame
12 weeks
Title
The number of days with migraine headache
Description
The number of days with migraine headache from baseline after treatment with Flunarizine vs Alpha Lipoic Acid
Time Frame
12 weeks
Title
The mean severity of acute attacks
Description
The mean severity of acute attacks will be considered as severity basis where 3 will be severe and 1 will be mild attack (on a 3-point scale: 3, severe; 2, moderate; 1, mild) from baseline after treatment with Flunarizine vs Alpha Lipoic Acid
Time Frame
12 weeks
Title
The number of days with nausea or vomiting
Description
The number of days with nausea or vomiting from baseline after treatment with Flunarizine vs Alpha Lipoic Acid
Time Frame
12 weeks
Title
The headache disability will be assessed by pedMIDAS (pediatric migraine disability assessment score)
Description
The headache disability will be assessed by pedMIDAS (pediatric migraine disability assessment score) scoring system (denotes 0 to 10 as little to no dyability and greater than 50 as severe disability) from baseline after treatment with Flunarizine vs Alpha Lipoic Acid
Time Frame
12 weeks
Title
The relapse rate among the responders after stoppage of prophylactic therapy .
Description
The relapse rate among the responders after stoppage of prophylactic therapy over the next 12 weeks.
Time Frame
12 weeks
Title
Serum thiol levels
Description
Serum thiol levels from baseline after treatment with Flunarizine vs Alpha Lipoic Acid
Time Frame
12 weeks
Title
Serum CGRP
Description
Serum CGRPlevels from baseline after treatment with Flunarizine vs Alpha Lipoic Acid
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with "15 or more headache days per month with at least 8 days having migraine features for at least 3 months (according to the criteria of the International Classification of Headache Disorders, 3rd edition [beta version], or ICHD-3 beta)." Adolescent migraineurs aged 10 to 19 years of age of either sex. Patients who have not taken any prophylactic treatment within the last three months before their inclusion in the study. Patients and/or parents have given informed written consent/assent. Exclusion Criteria: Patient with headache other than migraine. Patients who were on corticosteroids Treatment with any test drugs in the preceding three months from the start of the trial. If there is any history of interventions or devices used for the treatment of migraine, such as transcranial magnetic stimulation and nerve blocks during the 3 months before screening. Any other accompanying systemic illness; abnormalities revealed on neurologic examination. Psychiatric disturbances, history of epilepsy , learning disabilities, head trauma or use of other drugs acting on the central nervous system, including, smoking, alcohol consumption or any illicit drug abuse
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rituparna Maiti, MD
Organizational Affiliation
Additional Professor
Official's Role
Study Director
Facility Information:
Facility Name
AIIMS
City
Bhubaneswar
State/Province
Odisha
ZIP/Postal Code
751019
Country
India

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
28647791
Citation
Karsan N, Prabhakar P, Goadsby PJ. Premonitory Symptoms of Migraine in Childhood and Adolescence. Curr Pain Headache Rep. 2017 Jul;21(7):34. doi: 10.1007/s11916-017-0631-y.
Results Reference
background
PubMed Identifier
17550953
Citation
Eiland LS, Jenkins LS, Durham SH. Pediatric migraine: pharmacologic agents for prophylaxis. Ann Pharmacother. 2007 Jul;41(7):1181-90. doi: 10.1345/aph.1K049. Epub 2007 Jun 5.
Results Reference
background
PubMed Identifier
22500646
Citation
O'Brien HL, Kabbouche MA, Hershey AD. Treating pediatric migraine: an expert opinion. Expert Opin Pharmacother. 2012 May;13(7):959-66. doi: 10.1517/14656566.2012.677434. Epub 2012 Apr 14.
Results Reference
background
PubMed Identifier
28527067
Citation
D'Onofrio F, Raimo S, Spitaleri D, Casucci G, Bussone G. Usefulness of nutraceuticals in migraine prophylaxis. Neurol Sci. 2017 May;38(Suppl 1):117-120. doi: 10.1007/s10072-017-2901-1.
Results Reference
background
PubMed Identifier
23336811
Citation
Wang J, Tang J, Zhou X, Xia Q. Physicochemical characterization, identification and improved photo-stability of alpha-lipoic acid-loaded nanostructured lipid carrier. Drug Dev Ind Pharm. 2014 Feb;40(2):201-10. doi: 10.3109/03639045.2012.753901. Epub 2013 Jan 22.
Results Reference
background
PubMed Identifier
17355494
Citation
Magis D, Ambrosini A, Sandor P, Jacquy J, Laloux P, Schoenen J. A randomized double-blind placebo-controlled trial of thioctic acid in migraine prophylaxis. Headache. 2007 Jan;47(1):52-7. doi: 10.1111/j.1526-4610.2006.00626.x.
Results Reference
background
PubMed Identifier
3282670
Citation
Sorge F, De Simone R, Marano E, Nolano M, Orefice G, Carrieri P. Flunarizine in prophylaxis of childhood migraine. A double-blind, placebo-controlled, crossover study. Cephalalgia. 1988 Mar;8(1):1-6. doi: 10.1046/j.1468-2982.1988.0801001.x.
Results Reference
background
PubMed Identifier
30947525
Citation
Abu-Arafeh I, Hershey AD, Diener HC, Tassorelli C; Clinical Trials Standing Committee and the Child and Adolescent Standing Committee of the International Headache Society. Guidelines of the International Headache Society for controlled trials of preventive treatment of migraine in children and adolescents, 1st edition. Cephalalgia. 2019 Jun;39(7):803-816. doi: 10.1177/0333102419842188. Epub 2019 Apr 4.
Results Reference
background
PubMed Identifier
2861907
Citation
Sorge F, Marano E. Flunarizine v. placebo in childhood migraine. A double-blind study. Cephalalgia. 1985 May;5 Suppl 2:145-8. doi: 10.1177/03331024850050S227.
Results Reference
background
PubMed Identifier
26923752
Citation
Kenney D, Jenkins S, Youssef P, Kotagal S. Patient Use of Complementary and Alternative Medicines in an Outpatient Pediatric Neurology Clinic. Pediatr Neurol. 2016 May;58:48-52.e7. doi: 10.1016/j.pediatrneurol.2015.11.003. Epub 2016 Jan 11.
Results Reference
background

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Evaluation of Efficacy and Safety of add-on Alpha-lipoic Acid on Migraine Prophylaxis in Adolescent Population

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