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Trial · NCT07061847

Bilateral Middle Meningeal Artery Lidocaine Infusion for Chronic Debilitating Migraines

NCT07061847, Phase 2, Recruiting, Northwell Health

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Bilateral Middle Meningeal Artery Lidocaine Infusion for Chronic Debilitating Migraines. Trials, record NCT07061847. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07061847

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Bilateral Middle Meningeal Artery Lidocaine Infusion for Chronic Debilitating Migraines
NCT number
NCT07061847
Status
Recruiting
Phases
Phase 2
Enrollment
40 participants, estimated
Lead sponsor
Northwell Health
Conditions
Migraine
Interventions
Lidocaine (drug), Lidocaine Procedure
First posted
2025-07-11
Last updated
2026-05-22

Source ClinicalTrials.gov

Registered outcomes10

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryReduction in Monthly Migraine Headache DaysFrom enrollment to post-treatment at 3 monthsTo observe a ≥50% reduction in monthly migraine headache days in one month post intra-arterial lidocaine infusion into the bilateral middle meningeal artery.
Secondary≥50% reduction in migraine headache intensity at 15 minutes, 2 hours, and 24 hours post procedure.15 minutes, 2 hours, and 24 hours post-procedure.
SecondarySustained freedom from headache pain >48hrs.>48hrs post treatment
SecondaryPercentage of patients achieving ≥75% and 100% reduction in monthly headache days at 1 month and 3 monthsAt 1 month and 3 month post procedure
SecondaryMean number of monthly migraine headaches days at 1 month and 3 months.From enrollment to 1 month and 3 months post procedure
SecondaryMean change from baseline in the Global Assessment of Migraine Severity (GAMS) at 3 monthsFrom enrollment to 3 months post procedure
SecondaryPercent with improvement in Migraine Disability Assessment (MIDAS) at 3 months from severe disability (Grade IV, score ≥21) to no moderate disability (Grade I to III, score 0-21)From enrollment to 3 month post procedure
SecondaryPercent Headache Impact Test (HIT)-6 score <50 at 3 months.From enrollment to 3 months post procedure
SecondaryPercent with reduction in need for analgesic use by ≥50% at 3 months.From enrollment to 3 months post procedure
SecondaryAdverse events at 24 hours and 3 months post-procedure.From enrolllment to 3 months post procedure

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07061847

GET https://conductscience.org/api/trials/v1/NCT07061847/registered