Evaluation of Conventional and Long Pulse Widths During a Temporary Spinal Cord Stimulation Trial

Completed · Not applicable

Conditions studied: Spinal Cord Stimulation, Pain, Back, Pain

In brief

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

Key facts

Study ID

NCT03526055

Run by

Amol Soin

People needed

10

Starts

2018-02-26

Expected to finish

2018-05-31

Last updated by the study team

2019-02-21

Who can join

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

You may qualify if…

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

You may not qualify if…

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

Where it is running

• Ohio Pain Clinic — Centerville, Ohio, United States

Full record on ClinicalTrials.gov

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