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RECRUITING NA

MMA Embolization for Refractory Chronic Migraine

NCT06735833 · View on ClinicalTrials.gov ↗

Study Summary

This is a prospective, multi-center, feasibility study to investigate safety and effectiveness of TRUFILL n-BCA liquid embolic system in bilateral middle meningeal artery (MMA) embolization for the treatment of refractory chronic migraine.

Conditions Studied

Interventions

  • DEVICE Middle Meningeal Artery embolization

Study Locations (7)

New York

  • University of Buffalo Medical Center — Buffalo
  • Mount Sinai — New York
  • Stony Brook University Medical Center — Stony Brook

Connecticut

  • Hartford Hospital — Hartford

Pennsylvania

  • Thomas Jefferson University Hospital — Philadelphia

Tennessee

  • Semmes Murphey Foundation — Memphis

West Virginia

  • West Virginia University — Morgantown

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2025-04-23
Est. Completion 2029-05-15
Phase NA

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06735833

The ClinicalTrials.gov registry entry for NCT06735833 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 70 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cerenovus, Part of DePuy Synthes Products, which has 30 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Migraine appearing as the primary indexed condition, and to 1 intervention — of which Middle Meningeal Artery embolization is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06735833 reports 7 study locations spanning 5 distinct geographic areas — top geographies include New York, Connecticut, Pennsylvania. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06735833 about?

NCT06735833 is a clinical study titled "MMA Embolization for Refractory Chronic Migraine". This is a prospective, multi-center, feasibility study to investigate safety and effectiveness of TRUFILL n-BCA liquid embolic system in bilateral middle meningeal artery (MMA) embolization for the treatment of refractory chronic migraine.

What is the current status of trial NCT06735833?

This trial is currently recruiting. It is a NA study. The enrollment target is 70 participants. The study started on 2025-04-23. Estimated completion is 2029-05-15.

What conditions does trial NCT06735833 study?

This clinical trial studies the following conditions: Migraine. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06735833?

The interventions under investigation include: Middle Meningeal Artery embolization (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06735833?

This trial is sponsored by Cerenovus, Part of DePuy Synthes Products, which has 30 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06735833 being conducted?

This trial has 7 study locations across Connecticut, New York, Pennsylvania, Tennessee, West Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial