Brief Summary
This study will evaluate de-identified (anonymous) data in subject medical charts to review the clinical outcomes of various treatment approaches in the treatment of chronic pain.
Brief Title
Patient Retrospective Outcomes (PRO)
Detailed Description
This study is a retrospective, multi-center, de-identified patient data review.
The study will include multiple independent cohorts to evaluate clinical outcomes in different subgroups.
The study will include multiple independent cohorts to evaluate clinical outcomes in different subgroups.
Central Contacts
Central Contact Role
Contact
Central Contact Phone
855-213-9890
Central Contact Email
BSNClinicalTrials@bsci.com
Central Contact Role
Contact
Central Contact Phone
855-213-9890
Central Contact Email
BSNClinicalTrials@bsci.com
Completion Date
Completion Date Type
Estimated
Conditions
Chronic Pain
Eligibility Criteria
Key Inclusion Criteria:
* Previously treated with or eligible for use with Boston Scientific Systems
* 18 years of age or older at the start of Baseline
* Previously treated with or eligible for use with Boston Scientific Systems
* 18 years of age or older at the start of Baseline
Inclusion Criteria
Key Inclusion Criteria:
* Previously treated with or eligible for use with Boston Scientific Systems
* 18 years of age or older at the start of Baseline
* Previously treated with or eligible for use with Boston Scientific Systems
* 18 years of age or older at the start of Baseline
Gender
All
Gender Based
false
Healthy Volunteers
No
Last Update Post Date
Last Update Post Date Type
Actual
Last Update Submit Date
Minimum Age
18 Years
NCT Id
NCT01550575
Org Class
Industry
Org Full Name
Boston Scientific Corporation
Org Study Id
A7005
Overall Status
Recruiting
Primary Completion Date
Primary Completion Date Type
Estimated
Official Title
Patient Retrospective Outcomes (PRO)
Primary Outcomes
Outcome Description
Responder rate for pain relief through study completion.
Outcome Measure
Responder rate
Outcome Time Frame
Through study completion, approximately two years
Start Date
Start Date Type
Actual
Status Verified Date
First Post Date
First Post Date Type
Estimated
First Submit Date
First Submit QC Date
Study Population
Subjects who have previously been implanted with, or who are candidates for implantation with a spinal cord stimulation system or other various treatment approaches, such as radio frequency ablation or indirect decompression system (IDS).
Std Ages
Adult
Older Adult
Maximum Age Number (converted to Years and rounded down)
999
Minimum Age Number (converted to Years and rounded down)
18
Investigators
Investigator Type
Principal Investigator
Investigator Name
Sayed Wahezi
Investigator Email
swahezi@montefiore.org
Investigator Phone