Evaluation of Clinical Outcomes of Pulse Widths in Spinal Cord Stimulation

Completed · Not applicable

Conditions studied: Back Pain, Pain

In brief

The purpose of this study is to evaluate the effect of pulse widths \<500 μsec and \>1000 μsec on clinical outcomes during a temporary SCS trial.

Key facts

Study ID

NCT03756012

Run by

Kettering Health Network

People needed

15

Starts

2018-11-27

Expected to finish

2019-10-02

Last updated by the study team

2021-03-08

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• be eligible for SCS therapy according to the Algovita® SCS system Indications for Use statement
• be undergoing a SCS trial using Algovita® SCS system
• sign a valid, Institutional Review Board (IRB)-approved informed consent form.
• be 18 years of age or older when written informed consent is obtained

You may not qualify if…

• be contraindicated for an Algovita® SCS system
• have a cognitive impairment or exhibits any characteristic, that would limit the study candidate's ability to assess pain relief or complete study assessments
• have a life expectancy of less than 2 years
• be participating in another clinical study that would confound data analysis
• have a coexisting pain condition that might confound pain ratings
• have a significant psychiatric disorder

Where it is running

• The Ohio Pain Clinic — Centerville, Ohio, United States

Full record on ClinicalTrials.gov

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