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Sponsored by: |
Medtronic |
Information provided by: | Medtronic |
ClinicalTrials.gov Identifier: | NCT00157742 |
Randomised trial of Spinal Cord Stimulation (SCS) and Percutaneous Myocardial Laser Revascularisation (PMR) in patients with Refractory Angina Pectoris.
Hypothesis: difference in exercise tolerance at 12 months between SCS and PMR
Condition | Intervention | Phase |
Angina Pectoris |
Procedure: Spinal Cord Stimulation (SCS) Procedure: Percutaneous Myocardial Laser Revascularisation (PMR) |
Phase IV |
MedlinePlus related topics: | Angina Exercise and Physical Fitness |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study |
Official Title: | An Open Single-Centre Parallel Randomised Trial of Spinal Cord Stimulation (SCS) and Percutaneous Myocardial Revascularisation (PMR) in Patients With Refractory Angina Pectoris |
Estimated Enrollment: | 66 |
Study Start Date: | September 2000 |
Estimated Study Completion Date: | January 2007 |
The purpose of this open, parallel, single-center prospective, randomised controlled trial is to compare two treatments: Spinal Cord Stimulation (SCS) and Percutaneous Myocardial Laser Revascularisation (PMR) and assess their use and longer term effect in patients with Refractory Angina Pectoris.
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion criteria:
United Kingdom, Cambridge | |||||
Papworth Hospital | |||||
Papworth Everard, Cambridge, United Kingdom, CB3 8RE |
Medtronic |
Principal Investigator: | Peter Schofield, MD | Papworth Hospital, NHS |
Study ID Numbers: | SPIRIT |
First Received: | September 9, 2005 |
Last Updated: | December 15, 2005 |
ClinicalTrials.gov Identifier: | NCT00157742 |
Health Authority: | United Kingdom: National Health Service |
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