Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Boston Scientific Corporation
The purpose of this outcomes study is to compile real-world outcomes for the commercially approved Indirect Decompression Systems (IDS) in routine clinical practice when used according to the applicable Instructions for Use.
Age
21–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Scheduled to receive or previously received a commercially approved Boston Scientific Indirect Decompression Systems, per local Instructions for Use (IFU)
Signed a valid, IRB approved informed consent form
You may not be if
Meets any contraindication in BSC Indirect Decompression Systems local IFU
Clareo Health | Postmarket Outcomes Study for Evaluation of the Superion™ Spacer
