Skip to content

Comparing patient's preference of dorsal column stimulation versus dorsal root ganglion stimulation in patients with complex regional pain syndrome confined to the knee

Comparing patient's preference of dorsal column stimulation versus dorsal root ganglion stimulation in patients with complex regional pain syndrome confined to the knee - DCS/DRG Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON41087
Enrollment
15
Registered
2014-07-31
Start date
2014-09-16
Completion date
Unknown
Last updated
2024-06-11

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

Conditions

Complex Regional Pain Syndrome Reflex Sympathetic Dystrophy

Interventions

Placement of two different types of neurostimulation leads: corsal column stimulation leads and dorsal root ganglion stimulation leads. After the trial period of 16 days, the patient will undergo a

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Over one year CRPS confined to the knee, diagnosed according to the Budapest Criteria Set - Minimum age of 18 years - No improvement of symptoms after at least one year of treatment according to the Dutch guidelines for CRPS in primary care - Pain intensity of at least 50 mm measured on a visual analogue scale 0-100 mm

Exclusion criteria

Exclusion criteria: - Previous neurostimulation - Depression or an anxiety disorder - Pregnancy or pregnancy desire within one year - Patients who are not able to complete the questionnaires - Body Mass Index >35 - Life expectancy

Design outcomes

Primary

MeasureTime frame
The aim of this study is to compare the effect on chronic pain of two neurostimulation types; DCS and DRG stimulation in a group of patients with chronic pain due to CRPS confined to the knee. Primary objective will be the patient*s preference.

Secondary

MeasureTime frame
- Pain - Quality of life - Functionality of the affected limb - The effect on inflammation by stimulation Pain medication utilization will be recorded and tracked during the follow up.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)