At a glance
ClinicalIndex Comparison RecordN/ACompleted· 15 enrolled
Drug / intervention
Algovita Spinal Cord Stimulation Systemdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Multi-Center Evaluation of Clinical Outcomes of Pulse Widths <500 μsec and >1000 μsec During a Temporary Spinal Cord Stimulation Trial
In Brief
A clinical study evaluating Algovita Spinal Cord Stimulation System for Back Pain and Pain. Completed, enrolled 15 participants across 1 site.
Detailed Summary
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.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
CollaboratorsOhio Pain Clinic
Timeline
N/ACompletedFinished
20192020202120222023202420252026
Enrollment StartNov 2018
First PostedNov 2018
Primary CompletionOct 2019
TodayJul 2026
First PostedNov 28, 2018
Enrollment StartNov 27, 2018
Primary CompletionOct 2, 2019
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 7.6 years ago
Interventions
Algovita Spinal Cord Stimulation Systemdevice
The Algovita™ SCS system is indicated as an aid in the management of chronic intractable pain of the trunk and/or limbs, including unilateral or bilateral pain associated with failed back surgery syndrome, intractable low back pain and leg pain.