Migraine Disorders Clinical Trial
— LMMMOfficial title:
A Longitudinal Follow-up Study of the Patients With Medication-overuse Headache or Migraine That Completed Baseline MRI
This is a phone interview research study for patients with migraine or medication-overuse headache (MOH) who have completed baseline MRI scans. Participants will be interviewed by phone at 3, 12, 24 months after the baseline MRI scans. The purpose of this study is to potentially identify the baseline brain functional or structural signatures (functional connectivity, regional homogeneity, amplitude of low frequency fluctuation, and so such) that are predictive of the short- and long- term outcomes as well as treatment response of migraine and MOH patients.
Status | Recruiting |
Enrollment | 122 |
Est. completion date | October 31, 2025 |
Est. primary completion date | October 1, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: - Participants who are diagnosed with migraine or MOH at baseline visit, signed the consent form, and completed MRI scans. - Participants who are willing to take the phone interview during follow-up. Exclusion Criteria: - Refuse or unable to complete the phone interview procedure during follow-up. |
Country | Name | City | State |
---|---|---|---|
China | Chinese PLA General Hospital | Beijing | Beijing |
Lead Sponsor | Collaborator |
---|---|
Wei Dai | International Headache Society |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Monthly Number of Migraine Days | A migraine day is defined as a day with headache lasting at least 30 minutes without intake of analgesics and meeting ICHD-3 criteria for migraine or probable migraine. A migraine day may also be defined as a day with headache that successfully responds to acute treatment with a migraine-specific medication (triptan, ditan, gepant, ergotamine, etc.). | 3 months after the baseline MRI | |
Primary | Monthly Number of Migraine Days | A migraine day is defined as a day with headache lasting at least 30 minutes without intake of analgesics and meeting ICHD-3 criteria for migraine or probable migraine. A migraine day may also be defined as a day with headache that successfully responds to acute treatment with a migraine-specific medication (triptan, ditan, gepant, ergotamine, etc.). | 12 months after the baseline MRI | |
Primary | Monthly Number of Migraine Days | A migraine day is defined as a day with headache lasting at least 30 minutes without intake of analgesics and meeting ICHD-3 criteria for migraine or probable migraine. A migraine day may also be defined as a day with headache that successfully responds to acute treatment with a migraine-specific medication (triptan, ditan, gepant, ergotamine, etc.). | 24 months after the baseline MRI | |
Primary | Monthly Number of Moderate/Severe Headache Days | A moderate/severe headache day is defined as a day with headache pain of moderate or severe intensity that lasts at least 4 hours without medication, or a day with a headache pain of at least moderate intensity that responds to acute treatment with a migraine-specific medication. | 3 months after the baseline MRI | |
Primary | Monthly Number of Moderate/Severe Headache Days | A moderate/severe headache day is defined as a day with headache pain of moderate or severe intensity that lasts at least 4 hours without medication, or a day with a headache pain of at least moderate intensity that responds to acute treatment with a migraine-specific medication. | 12 months after the baseline MRI | |
Primary | Monthly Number of Moderate/Severe Headache Days | A moderate/severe headache day is defined as a day with headache pain of moderate or severe intensity that lasts at least 4 hours without medication, or a day with a headache pain of at least moderate intensity that responds to acute treatment with a migraine-specific medication. | 24 months after the baseline MRI | |
Primary | Severity of Headache Measured by Visual Analogue Scale | Severity of headache is measured by VAS ranging from 0 to 10 with 1 = most mild to 10 = most severe. The mean severity of headache for each month will be calculated as: sum of severity of headache days divided by number of headache days. | 3 months after the baseline MRI | |
Primary | Severity of Headache Measured by Visual Analogue Scale | Severity of headache is measured by VAS ranging from 0 to 10 with 1 = most mild to 10 = most severe. The mean severity of headache for each month will be calculated as: sum of severity of headache days divided by number of headache days. | 12 months after the baseline MRI | |
Primary | Severity of Headache Measured by Visual Analogue Scale | Severity of headache is measured by VAS ranging from 0 to 10 with 1 = most mild to 10 = most severe. The mean severity of headache for each month will be calculated as: sum of severity of headache days divided by number of headache days. | 24 months after the baseline MRI | |
Primary | Mean Headache Duration (hours) | As a feature of the headache attack duration. | 3 months after the baseline MRI | |
Primary | Mean Headache Duration (hours) | As a feature of the headache attack duration. | 12 months after the baseline MRI | |
Primary | Mean Headache Duration (hours) | As a feature of the headache attack duration. | 24 months after the baseline MRI | |
Primary | Nausea (number) | As a feature of the accompany symptoms during an attack. | 3 months after the baseline MRI | |
Primary | Nausea (number) | As a feature of the accompany symptoms during an attack. | 12 months after the baseline MRI | |
Primary | Nausea (number) | As a feature of the accompany symptoms during an attack. | 24 months after the baseline MRI | |
Primary | Vomiting (number) | As a feature of the accompany symptoms during an attack. | 3 months after the baseline MRI | |
Primary | Vomiting (number) | As a feature of the accompany symptoms during an attack. | 12 months after the baseline MRI | |
Primary | Vomiting (number) | As a feature of the accompany symptoms during an attack. | 24 months after the baseline MRI | |
Primary | Photophobia (number) | As a feature of the accompany symptoms during an attack. | 3 months after the baseline MRI | |
Primary | Photophobia (number) | As a feature of the accompany symptoms during an attack. | 12 months after the baseline MRI | |
Primary | Photophobia (number) | As a feature of the accompany symptoms during an attack. | 24 months after the baseline MRI | |
Primary | Phonophobia (number) | As a feature of the accompany symptoms during an attack. | 3 months after the baseline MRI | |
Primary | Phonophobia (number) | As a feature of the accompany symptoms during an attack. | 12 months after the baseline MRI | |
Primary | Phonophobia (number) | As a feature of the accompany symptoms during an attack. | 24 months after the baseline MRI | |
Primary | Aggravation by Movement (number) | As a feature of the accompany symptoms during an attack. | 3 months after the baseline MRI | |
Primary | Aggravation by Movement (number) | As a feature of the accompany symptoms during an attack. | 12 months after the baseline MRI | |
Primary | Aggravation by Movement (number) | As a feature of the accompany symptoms during an attack. | 24 months after the baseline MRI | |
Primary | Response to Acute Treatment | To describe response to prior acute medications. | 3 months after the baseline MRI | |
Primary | Response to Acute Treatment | To describe response to prior acute medications. | 12 months after the baseline MRI | |
Primary | Response to Acute Treatment | To describe response to prior acute medications. | 24 months after the baseline MRI | |
Primary | Response to Prophylactic Treatment | To describe response to prior prophylactic medications. | 3 months after the baseline MRI | |
Primary | Response to Prophylactic Treatment | To describe response to prior prophylactic medications. | 12 months after the baseline MRI | |
Primary | Response to Prophylactic Treatment | To describe response to prior prophylactic medications. | 24 months after the baseline MRI | |
Primary | Migraine Disability Assessment Test Total Score | The MIDAS was designed to quantify headache-related disability over a 3-month period. This instrument consists of 5 items that measures the impact that migraine headaches have on patients' life, including days of work/school missed, days with productivity at work/school reduced to half or more, days with household work missed, days with productivity in household work reduced to half or more, and days missed family/social/leisure activities. Each item has a numeric response range from 0 to 90 days; if days are missed from work/school or household work they are not counted as days with reduced productivity at work/school or household work. The numeric responses are summed to produce a total score ranging from 0 to 270. A higher value is indicative of more disability. | 3 months after the baseline MRI | |
Primary | Migraine Disability Assessment Test Total Score | The MIDAS was designed to quantify headache-related disability over a 3-month period. This instrument consists of 5 items that measures the impact that migraine headaches have on patients' life, including days of work/school missed, days with productivity at work/school reduced to half or more, days with household work missed, days with productivity in household work reduced to half or more, and days missed family/social/leisure activities. Each item has a numeric response range from 0 to 90 days; if days are missed from work/school or household work they are not counted as days with reduced productivity at work/school or household work. The numeric responses are summed to produce a total score ranging from 0 to 270. A higher value is indicative of more disability. | 12 months after the baseline MRI | |
Primary | Migraine Disability Assessment Test Total Score | The MIDAS was designed to quantify headache-related disability over a 3-month period. This instrument consists of 5 items that measures the impact that migraine headaches have on patients' life, including days of work/school missed, days with productivity at work/school reduced to half or more, days with household work missed, days with productivity in household work reduced to half or more, and days missed family/social/leisure activities. Each item has a numeric response range from 0 to 90 days; if days are missed from work/school or household work they are not counted as days with reduced productivity at work/school or household work. The numeric responses are summed to produce a total score ranging from 0 to 270. A higher value is indicative of more disability. | 24 months after the baseline MRI | |
Primary | Patient Health Questionnaire 9 Depression Scale Total Score | The PHQ-9 was designed to identify signs or symptoms of depression over a two-week period. The total score is calculated and can range from zero to 27. Scores of 5, 10, 15, and 20 are taken as the cut-off points for mild, moderate, moderate to severe, and severe depression, respectively. | 3 months after the baseline MRI | |
Primary | Patient Health Questionnaire 9 Depression Scale Total Score | The PHQ-9 was designed to identify signs or symptoms of depression over a two-week period. The total score is calculated and can range from zero to 27. Scores of 5, 10, 15, and 20 are taken as the cut-off points for mild, moderate, moderate to severe, and severe depression, respectively. | 12 months after the baseline MRI | |
Primary | Patient Health Questionnaire 9 Depression Scale Total Score | The PHQ-9 was designed to identify signs or symptoms of depression over a two-week period. The total score is calculated and can range from zero to 27. Scores of 5, 10, 15, and 20 are taken as the cut-off points for mild, moderate, moderate to severe, and severe depression, respectively. | 24 months after the baseline MRI | |
Primary | Generalized Anxiety Disorder Assessment 7-item Scale Total Score | The GAD-7 was designed to identify signs or symptoms of anxiety over a two-week period. The total score is calculated and can range from zero to 21. Scores of 5, 10, 14, and 19 are taken as the cut-off points for mild, moderate, moderate to severe, and severe anxiety, respectively. | 3 months after the baseline MRI | |
Primary | Generalized Anxiety Disorder Assessment 7-item Scale Total Score | The GAD-7 was designed to identify signs or symptoms of anxiety over a two-week period. The total score is calculated and can range from zero to 21. Scores of 5, 10, 14, and 19 are taken as the cut-off points for mild, moderate, moderate to severe, and severe anxiety, respectively. | 12 months after the baseline MRI | |
Primary | Generalized Anxiety Disorder Assessment 7-item Scale Total Score | The GAD-7 was designed to identify signs or symptoms of anxiety over a two-week period. The total score is calculated and can range from zero to 21. Scores of 5, 10, 14, and 19 are taken as the cut-off points for mild, moderate, moderate to severe, and severe anxiety, respectively. | 24 months after the baseline MRI | |
Primary | Quality and Patterns of Sleep Using Pittsburgh Sleep Quality Index Total Score | The PSQI is to assess sleep quality and disturbances over a 1-month time interval. Nineteen individual items generate seven component scores: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleeping medication, and daytime dysfunction. The sum of scores for the seven components yields one global score. Each item is weighted on a 0-3 interval scale. The global PSQI score is then calculated by totaling the seven component scores, providing an overall score ranging from 0 to 21, where lower scores denote a healthier sleep quality. | 3 months after the baseline MRI | |
Primary | Quality and Patterns of Sleep Using Pittsburgh Sleep Quality Index Total Score | The PSQI is to assess sleep quality and disturbances over a 1-month time interval. Nineteen individual items generate seven component scores: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleeping medication, and daytime dysfunction. The sum of scores for the seven components yields one global score. Each item is weighted on a 0-3 interval scale. The global PSQI score is then calculated by totaling the seven component scores, providing an overall score ranging from 0 to 21, where lower scores denote a healthier sleep quality. | 12 months after the baseline MRI | |
Primary | Quality and Patterns of Sleep Using Pittsburgh Sleep Quality Index Total Score | The PSQI is to assess sleep quality and disturbances over a 1-month time interval. Nineteen individual items generate seven component scores: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleeping medication, and daytime dysfunction. The sum of scores for the seven components yields one global score. Each item is weighted on a 0-3 interval scale. The global PSQI score is then calculated by totaling the seven component scores, providing an overall score ranging from 0 to 21, where lower scores denote a healthier sleep quality. | 24 months after the baseline MRI |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT01432379 -
BOTOX® Prophylaxis in Patients With Chronic Migraine
|
||
Completed |
NCT04084314 -
Assessment of Prolonged Safety and tOLerability of in Migraine Patients in a Long-term OpeN-label Study
|
Phase 4 | |
Recruiting |
NCT05048914 -
Migraine Abortive Treatment
|
||
Completed |
NCT03662295 -
Stroke-like Migraine Attacks After Radiation Treatment (SMART) Syndrome Language Intervention
|
||
Completed |
NCT02766517 -
Biomarker Study in Participants With Migraine
|
Early Phase 1 | |
Completed |
NCT00963937 -
Study to Evaluate the Efficacy and Safety of Oral Sumatriptan for the Acute Treatment of Migraine in Children and Adolescents
|
Phase 3 | |
Not yet recruiting |
NCT03632928 -
Day to Day Variation of Pressure Pain Threshold and Muscle Hardness
|
||
Completed |
NCT02559895 -
A Multicenter Assessment of ALD403 in Frequent Episodic Migraine
|
Phase 3 | |
Completed |
NCT01435941 -
Non-steroidal Anti-inflammatory Drugs Alone or With a Triptan and Reports of Transition From Episodic to Chronic Migraine
|
N/A | |
Completed |
NCT00743015 -
Relative Bioavailability of a Single Dose of BI 44370 Tablet During and Between Migraine Attacks
|
Phase 1 | |
Completed |
NCT01376141 -
Drug Use Investigation for IMIGRAN Tablet
|
N/A | |
Completed |
NCT02183688 -
Acetylsalicylic Acid (ASA) + Paracetamol + Caffeine Combination Compared With ASA + Paracetamol as Well as ASA, Paracetamol, and Caffeine in Headache Patients
|
Phase 3 | |
Completed |
NCT06061588 -
"Potential Effects of Virtual Reality Technology on the Treatment of Migraine-Type Headaches"
|
N/A | |
Completed |
NCT03588364 -
The Role of Osteopathic Manipulation in the the Management of Post-traumatic Migraine
|
N/A | |
Completed |
NCT04091321 -
Association Between Chronic Headache and Back Pain With Childbirth
|
||
Completed |
NCT00385008 -
TREXIMA and RELPAX Gastric Scintigraphy Inside and Outside a Migraine
|
Phase 3 | |
Active, not recruiting |
NCT05888298 -
Proximal and Distal Approach GON RFT in Migraine
|
N/A | |
Completed |
NCT03435185 -
Greater Occipital and Supraorbital Nerve Blockade in Migraine Patients
|
N/A | |
Recruiting |
NCT06459635 -
Migraine Attack Pain Phase Prediction Study
|
||
Completed |
NCT02565186 -
An Open-label, Long-term, Safety Study of Lasmiditan for the Acute Treatment of Migraine
|
Phase 3 |