Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 10:21 PM
Ignite Modification Date:
2025-12-24 @ 10:21 PM
NCT ID:
NCT04765735
Eligibility Criteria:
Inclusion Criteria:
* 22 years of age or older
* Candidate for or undergoing Medtronic SCS device trial for labeled indication - Candidate for or undergoing a Medtronic SCS device trial for labeled indication means that a clinical decision has already been made between a physician and the patient to undergo Medtronic SCS trialing to treat the patient's chronic pain. This decision is to be made prior to discussing with the patient whether to enroll in the study
* Willing and able to provide signed and dated informed consent
* Capable of comprehending and consenting in English
* Willing and able to comply with all study procedures and visits
* Clear, measurable ECAP ECAPs - If during set up of the in-clinic testing, the subject does not have a clear, measurable ECAP (\>10uV amplitude obtained consistently and repeatably) they will not move forward with testing or randomization and will be considered a screen failure.
Exclusion Criteria:
* Implanted electrical cardiac devices (e.g., pacemaker, defibrillator)
* Currently enrolled or planning to enroll in an interventional clinical study that could potentially confound the study results (co-enrollment in an interventional study is only allowed when documented pre-approval is obtained from the Medtronic study manager or designee)
* Pregnant or is of child-bearing potential and unwilling to use a medically acceptable form of birth control during the study
* Has untreated major psychiatric comorbidity, as determined by the investigator or designee
* Trialed with a permanent implant lead and extension ("buried lead trial")
* If subject is classified as vulnerable or requires a legally authorized representative (LAR)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
22 Years
Study:
NCT04765735
Study Brief:
Protocol Section:
NCT04765735