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Behavioural Intervention
NeuroMetrix for Peripheral Neuropathy
N/A
Waitlist Available
Led By Hye Sook Chon, MD
Research Sponsored by H. Lee Moffitt Cancer Center and Research Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline to 30 days after 3 week treatment sessions
Awards & highlights
Study Summary
This trial will test the validity of a new, point-of-care nerve conduction device and a common tuning fork in assessing the level of chemotherapy-induced peripheral neuropathy in patients.
Eligible Conditions
- Peripheral Neuropathy
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline to 30 days after 3 week treatment sessions
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline to 30 days after 3 week treatment sessions
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Accessing Level of Peripheral Neuropathy
Secondary outcome measures
Nail-Patella Syndrome
Quality of life Improvement measured with FACT/GOG-NTX Questionnaire
Trial Design
1Treatment groups
Experimental Treatment
Group I: Participants Receiving ElectroacupunctureExperimental Treatment3 Interventions
Participants will receive electroacupuncture for 30 minutes once per week for a total of 3 weeks.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
NeuroMetrix
2020
N/A
~30
Electroacupuncture
2012
Completed Phase 3
~1800
Rydel-Seiffer tuning fork
2020
N/A
~30
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Who is running the clinical trial?
H. Lee Moffitt Cancer Center and Research InstituteLead Sponsor
542 Previous Clinical Trials
135,469 Total Patients Enrolled
Hye Sook Chon, MDPrincipal InvestigatorMoffitt Cancer Center
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