Acupuncture for Epilepsy in Patients with RNS Systems

This study is exploring whether acupuncture can help people with epilepsy who have a Responsive Neurostimulation System (RNS) implanted. Researchers want to see if 12 weeks of acupuncture treatment can reduce the number and severity of your seizures, improve your mood and thinking, and affect the electrical activity in your brain as recorded by the RNS system. You may be able to join if you are between 15 and 60 years old, have an RNS system, and can keep your current medications and RNS settings stable for 12 weeks. The study is looking for 10 participants, but its current recruitment status is unclear.

Study design
This is an interventional study with a planned enrollment of 10 participants. It is not specified if the study is randomized or blinded.
What's involved
You would receive one 40-minute to one-hour acupuncture session per week for 12 weeks. You would also need to maintain stable medications and RNS settings for 12 weeks.
Compensation
Not stated in the trial record.
Follow-up
Your seizure frequency and severity will be measured at baseline and again 12 weeks after treatment.

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NCT04677751

Clinical and Electrographic Changes in Responsive Neurostimulation System (RNS) Patients with Acupuncture Treatment

UNKNOWN
NAAges 15–60InterventionalSupportive care
The University of Texas Health Science Center, Houston
~10 participants
Updated 2024-10-01 on ClinicalTrials.gov
What's tested:Acupuncture intervention

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Percent change in number of disabling clinical seizures
Measured over Baseline,12 weeks post treatment
+1 more outcome measured
Epilepsy
1 sites across 1 states
Texas1
  • Olga Rodziyevska, MS,PA-C · PRINCIPAL_INVESTIGATOR · The University of Texas Health Science Center, Houston

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Eligibility criteria

Inclusion

Patient implanted with the RNS system
Patient can undergo 12 weeks of acupuncture
Patient is able remain on stable medications for 12 weeks
Patient is able to remain on stable Detection and Stimulation settings for 12 weeks
Patient or/and caregiver is able to understand and sign informed consent and HIPAA authorization
Patient or caregiver able to maintain a seizure diary for duration of study

Exclusion

Patient and /or caregiver is unable to sign informed consent to study
Patient has a bleeding disorder, pacemaker, or pregnant
  • Percent change in number of disabling clinical seizuresBaseline,12 weeks post treatment

    This will be measured by self reporting journals

  • Changes in seizure severityBaseline,12 weeks post treatment

    This will be measured by self reporting journals