Patient satisfaction with stimulation sensation and coverage comparing single versus dual channel stimulation in the Synergy ® system

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN32625089

Enrollment

Registered

2006-09-29

Start date

2005-10-01

Completion date

Unknown

Last updated

2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Signs and Symptoms: Pain Signs and Symptoms Pain

Interventions

20 patients already implanted with Synergy Spinal Cord Stimulation (SCS) device for pain relief will be recruited. Baseline data will be collected for paraesthesia coverage and patient satisfaction (

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient implanted with Synergy stimulator 2. Patient willing to take part in the study

Exclusion criteria

Exclusion criteria: 1. Patient implanted with single channel stimulator 2. Patient unwilling to take part in the study

Design outcomes

Primary

Measure	Time frame
1. Patient satisfaction score (0-100mm line) 2. Paraesthesia coverage (0-100mm line) 3. Global perceived effect (1-7)	—

Secondary

Measure	Time frame
Not provided at time of registration	—

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026