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Study identifier: NCT07309874 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Effect of Ultrasound-Guided Dry Needling Targeting Rectus Capitus Posterior Major on Individuals With Headaches

Condition: Headache Disorders, Primary · Headache, Cervicogenic  ·  Sponsor: Texas Tech University Health Sciences Center

PhaseNA
Planned participants50
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

Headaches such as tension-type, migraine, and cervicogenic (neck-related) headaches are among the most common and disabling conditions worldwide. and are often associated with tight or sensitive muscles at the base of the skull, which can contribute to headaches. Dry needling involves inserting a very thin, sterile needle into tight muscle areas known as trigger points to relieve pain and muscle tension. When applied to the deep neck muscles, including those beneath the skull, dry needling may reduce headache symptoms. The suboccipital region contains important structures such as the vertebral artery, greater occipital nerve, and spinal cord, which requires precise needle placement to maintain safety. Many needling techniques used in this region have not been validated for accuracy or safety in living subjects. This study will use real-time ultrasound imaging to guide dry needling of the rectus capitis posterior major muscle and directly visualize nearby structures to minimize risk. The main goals of this research are to examine the effects of a single session of ultrasound-guided dry needling on headache symptoms and to confirm the safety, accuracy, and consistency of the proposed needling technique using ultrasound imaging.

This description comes directly from the study's public registry record.

Talk to the study team

Gary A Kearns, PT, ScD  ·  12142448398  ·  gary.kearns@ttuhsc.edu

Jace A Brown, PT, PhD  ·  9406897716  ·  jbrown34@twu.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Texas Tech University Health Sciences CenterLubbock, Texas, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07309874