An interventional study of Abbott® DRG / Abbott®/Medtronic® SCS and Control Group in Neuropathy;Peripheral, sponsored by M.D. Anderson Cancer Center. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-02.
Sponsored by M.D. Anderson Cancer Center · Not applicable, Interventional, and Treatment
To learn if a process called neuromodulation can help to improve pain due to CIP
Inclusion Criteria:
Exclusion Criteria:
73 studies on the registry are indexed under Neuritis; 20 are open to participants now.
This study's planned enrollment of 24 is below the median of 48 across 51 interventional studies indexed under Neuritis.
Browse Neuritis studies →M.D. Anderson Cancer Center is the lead sponsor of 3,047 studies on the registry; 578 are open to participants now.
Of its 612 completed or terminated interventional studies of FDA-regulated products, 409 (67%) have results posted.
Counted across the registry records on this site, refreshed daily.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Group 1 will receive neuromodulation.
Device: Abbott® DRG / Abbott®/Medtronic® SCS
Group 2 will not receive neuromodulation.
Other: Control Group
Participants will receive 1 of 2 neuromodulation procedures based on if participants are expected to have an MRI in the near future.
Participants will not receive any intervention
Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0
Time frame: through study completion; an average of 1 year.
From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗
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