Epilepsy Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- The person has already had the RNS system (a brain stimulation device) surgically implanted.
- The person is able to attend and complete 12 weeks of acupuncture sessions.
- The person is able to stay on the same medications without changes for 12 weeks.
- The person is able to keep their RNS device settings unchanged for 12 weeks.
- The person, or their caregiver, is able to understand and sign the consent and privacy forms required to participate.
- The person, or their caregiver, is able to keep a diary tracking seizures throughout the study.
Who may not be able to join:
- The person and their caregiver are unable to sign the required consent forms for the study.
- The person has a bleeding disorder, has a pacemaker, or is pregnant.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Olga Rodziyevska, MS,PA-C, The University of Texas Health Science Center, Houston
Phone: (713) 500-5482
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Percent change in number of disabling clinical seizures; Changes in seizure severity
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.