A Study to Determine the Effectiveness of Spinal Cord Stimulation for the Treatment of Refractory Angina Pectoris

Overview

About this study

The purpose of this study is to perform an in-depth review of pre-operative considerations and indications for spinal cord stimulation (SCS) for refractory angina pectoris (RAP), intraoperative findings, and postoperative reports of any adverse events and (secondarily) patient reports of effectiveness with this therapy.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. If you need assistance understanding the eligibility criteria, please contact the study team.

Inclusion Criteria:

  • All Mayo Clinic-Rochester patients who have undergone spinal cord stimulation for chest pain, chest tightness, or angina between January 1, 2003 and September 11, 2018.

Exclusion Criteria: 

  • Any children, prisoners, adults lacking capacity to consent, or patients who have declined research authorization.

Participating Mayo Clinic locations

Study statuses change often. Please contact us for help.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

William Mauck, M.D.

Closed for enrollment

Contact information:

William Mauck M.D.

(507) 284-9885

Mauck.William@mayo.edu

More information

Publications

Publications are currently not available

Study Results Summary

Not yet available

Supplemental Study Information

Not yet available

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CLS-20450616

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