This study is evaluating a minimally invasive treatment for adults with chronic neck pain and cervicogenic headaches that have not improved with conservative treatments. The goal is to better understand long-term pain relief and improvements in daily function after treatment.

Participants who qualify for the procedure will undergo a treatment designed to target nerves associated with chronic neck pain and headache symptoms.

Participants will be followed over time with visits at approximately:

• 1 month
• 3 months
• 6 months
• 12 months

At these visits, participants may:

• Complete questionnaires about pain and quality of life
• Discuss symptom improvement with the study team
• Review medication use and daily functioning

You may qualify if you:

• Are 18 years or older
• Have chronic neck pain and headaches lasting at least 6 months
• Have not improved with prior treatments such as medications, physical therapy, or other conservative care
• Previously experienced temporary relief from diagnostic nerve block procedures

You may not qualify if you:

• Are pregnant
• Have certain bleeding disorders or require long-term blood thinners
• Have uncontrolled psychiatric conditions
• Have had certain prior neck surgeries