Trials / Completed
CompletedNCT04909593
Study to Evaluate Automated Intensity Management in Patients Undergoing a BSC SCS Temporary Trial
Study to Evaluate Automated Intensity Management in Patients Undergoing a BSC SCS Temporary Trial: The AIM Study
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 21 (actual)
- Sponsor
- Boston Scientific Corporation · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of the study is to assess the feasibility of using information extracted from physiologic signals to automatically adjust stimulation in patients undergoing Spinal Cord Stimulation (SCS).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Spinal Cord Stimulation | Spinal cord stimulation at varied electrode, pulse width, frequency and amplitude parameters |
Timeline
- Start date
- 2021-05-24
- Primary completion
- 2022-11-22
- Completion
- 2022-11-22
- First posted
- 2021-06-02
- Last updated
- 2024-12-06
- Results posted
- 2024-12-06
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT04909593. Inclusion in this directory is not an endorsement.