Spinal Cord Stimulation (SCS) in Refractory Angina

Phase 4

• Conditions: Angina Pectoris
• Interventions: Device: Spinal cord stimulation

• Registration Number: NCT00121654
• Lead Sponsor: Catholic University of the Sacred Heart

Brief Summary

The study aims at assessing safety and efficacy of Spinal Cord Stimulation (SCS) for the treatment of refractory angina pectoris in a single blind, prospective, multicenter study.

Sixty patients with refractory angina with new SCS device implantation will be randomized to one of three treatment groups:

* paresthesic SCS;

* subliminal SCS;

* low (non effective) stimulation (control).

Clinical follow-up will be done at 1 and 3 months. Control group patients will then be randomized to paresthesic SCS or subliminal SCS for another 3 months and the 2 groups will be reassessed at 6 months.

Detailed Description

Aim of the study is to assess safety and efficacy of Spinal Cord Stimulation (SCS) for the treatment of refractory angina pectoris in a single blind, prospective, multicenter study. The study also assesses whether subliminal SCS may be as effective as paresthesic SCS in these patients.

Sixty consecutive patients with refractory angina with a new SCS device implantation will be randomized to one of three treatment groups:

* paresthesic SCS (group 1);

* subliminal SCS (75-80% of paresthesic threshold; group 2);

* low stimulation, consisting of an hour of SCS a day at 0.05 mV intensity, which does not have any significant stimulator effect (sham stimulation, group 3).

Study Procedure

Medical history, clinical data, drug therapy, Angina Canadian Cardiovascular Society (CCS) classification, Seattle Angina Questionnaire (SAQ), quality of life estimation by EuroQoL scale, detailed evaluation of angina attacks (frequency, intensity, duration of episodes; nitrates assumption) according to a structured diary, number of hospitalizations, emergency room (ER) admissions and cardiological visits in the previous 6 months and treadmill exercise stress test results will be obtained at the baseline visit.

Patients fulfilling inclusion criteria will undergo SCS implant. During the implant, stimulation tests will be performed to check paresthesic coverage of angina pain chest area.

Patients with adequate paresthesias will be randomized to one of the 3 groups. Follow-up visits will be performed at 1, 3, 6, and 12 months after the SCS implant. Drug therapy will not be changed at least during the first 3 months.

Patients assigned to group 2 (subliminal SCS) and those assigned to group 3 (sham SCS) will be blinded about the assigned treatment.

After the 3 months group 3, patients will be randomized to group 1 or group 2 and reassessed at 6-month follow-up (comparison between paresthesic versus subliminal SCS).

The controlled study will end at the 6-month follow-up, when each investigator will decide for the best stimulation for individual patients. Every patient will then be followed until 12 months from SCS implant.

Clinical assessment will be done at each follow-up visit. Exercise stress test results will be repeated at 3-, 6- and 12-month follow-up visits.

Study Timeline

• Study Start: 2005-07
• Study First Submitted: 2005-07-14
• Study First Submitted QC: 2005-07-14
• Study First Posted: 2005-07-21
• Primary Completion: 2008-12
• Status Verified: 2009-03
• Last Update Submitted: 2009-03-09
• Last Update Posted: 2009-03-10
• Study Completion: 2009-12

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• Stable angina pectoris refractory to optimal medical therapy, with at least 10 angina episodes in the three weeks previous SCS implant;
• Documentation of coronary artery disease and reversible myocardial ischaemia;
• Patient is not a candidate for or refuses surgical or percutaneous coronary revascularization;
• Availability for follow-up visits;
• Written informed consent.

Exclusion Criteria

• Severe spinal cord diseases that prevent the catheter positioning in the epidural space;
• No paresthesic coverage of angina pain area during SCS;
• Unstable angina pectoris;
• Female patients in fertile age;
• Enrolment in other studies;
• Need for anticoagulant therapy;
• Patients needing diathermy treatment;
• Life expectancy <12 months.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
1	Spinal cord stimulation	paresthesic SCS
2	Spinal cord stimulation	subliminal SCS (75-80% of paresthesic threshold)
3	Spinal cord stimulation	low stimulation, consisting of an hour of SCS a day at 0.05 mV intensity, which does not have any significant stimulator effect (sham stimulation)

Primary Outcome Measures

Name	Time	Method
Reduction of angina symptoms	1, 3, 6 and 12 months
improvement of quality of life	1, 3, 6 and 12 months

Secondary Outcome Measures

Name	Time	Method
Improvement of exercise induced myocardial ischemia	3, 6 and 12 months
evaluation of adverse events and complications	0, 1, 3, 6 and 12 months

Trial Locations

Locations (1)

Istituto di Cardiologia - Università Cattolica del Sacro Cuore; 🇮🇹 Roma, Italy