Actively Recruiting
Clinical and Electrographic Changes in Responsive Neurostimulation System (RNS) Patients with Acupuncture Treatment
Led by The University of Texas Health Science Center, Houston · Updated on 2024-10-01
10
Participants Needed
1
Research Sites
243 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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
CONDITIONS
Official Title
Clinical and Electrographic Changes in Responsive Neurostimulation System (RNS) Patients with Acupuncture Treatment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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
You will not qualify if you...
- Patient and /or caregiver is unable to sign informed consent to study
- Patient has a bleeding disorder, pacemaker, or pregnant
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The University of Texas Health Science Center at Houston
Houston, Texas, United States, 77030
Actively Recruiting
Research Team
O
Olga Rodziyevska, MS,PA-C
CONTACT
A
Ardonia N Tousant
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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