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Recruiting NCT04677751

NCT04677751 Clinical and Electrographic Changes in Responsive Neurostimulation System (RNS) Patients With Acupuncture Treatment

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Clinical Trial Summary
NCT ID NCT04677751
Status Recruiting
Phase —
Sponsor The University of Texas Health Science Center, Houston
Condition Epilepsy
Study Type INTERVENTIONAL
Enrollment 10 participants
Start Date 2021-04-01
Primary Completion 2027-12-30

Eligibility & Interventions

Sex All sexes
Min Age 15 Years
Max Age 60 Years
Study Type INTERVENTIONAL
Interventions
Acupuncture intervention

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 10 participants in total. It began in 2021-04-01 with a primary completion date of 2027-12-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The purpose of this study is to determine effects of Acupuncture on a Patient's mood and cognition,evaluate changes in clinically-reported seizure frequency and severity and analyze effects of Acupuncture on electrographic epileptiform activity stored by the RNS System

Eligibility Criteria

Inclusion Criteria: * 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 Criteria: * Patient and /or caregiver is unable to sign informed consent to study * Patient has a bleeding disorder, pacemaker, or pregnant

Contact & Investigator

Central Contact

Olga Rodziyevska, MS,PA-C

✉ Olga.Rodziyevska@uth.tmc.edu

📞 (713) 500-5482

Principal Investigator

Olga Rodziyevska, MS,PA-C

PRINCIPAL INVESTIGATOR

The University of Texas Health Science Center, Houston

Frequently Asked Questions

Who can join the NCT04677751 clinical trial?

This trial is open to participants of all sexes, aged 15 Years or older, up to 60 Years, studying Epilepsy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT04677751 currently recruiting?

Yes, NCT04677751 is actively recruiting participants. Contact the research team at Olga.Rodziyevska@uth.tmc.edu for enrollment information.

Where is the NCT04677751 trial being conducted?

This trial is being conducted at Houston, United States.

Who is sponsoring the NCT04677751 clinical trial?

NCT04677751 is sponsored by The University of Texas Health Science Center, Houston. The principal investigator is Olga Rodziyevska, MS,PA-C at The University of Texas Health Science Center, Houston. The trial plans to enroll 10 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology