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Stimulation Change Effects on Quantitative Sensory Testing in Neuromodulation Patients

NCT04708392 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 16

Last updated 2021-01-15

No results posted yet for this study

Summary

This study is designed to evaluate the effectiveness of two types of spinal cord stimulation programming types, in comparison to each other as well as patient baseline data.

Conditions

Interventions

DEVICE

Spinal Cord Stimulator

A spinal cord stimulator is a surgically implanted device that delivers an electrical signal to a patient's spinal cord to reduce the perception of pain

Sponsors & Collaborators

  • Albany Medical College

    lead OTHER

Principal Investigators

  • Julie Pilitsis, MD, PhD · AMC Department of Neurosurgery

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-07-29
Primary Completion
2018-07-31
Completion
2018-09-11
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04708392 on ClinicalTrials.gov