Effect of Spinal Cord Stimulation in Painful Diabetic Polyneuropathy

Diabetic Neuropathies Clinical Trial

— SCS  

Official title:

Effect of Spinal Cord Stimulation in Painful Diabetic Polyneuropathy (PDP Study) A Pilot Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00802022
• Other study ID #: MEC 08-2-118
• Status: Completed
• Phase: N/A
• First received: December 3, 2008
• Last updated: July 7, 2010
• Start date: January 2009
• Est. completion date: July 2010

Study information

• Verified date: July 2010
• Source: Maastricht University Medical Center
• Contact: n/a
• Is FDA regulated: No
• Health authority: Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)
• Study type: Interventional

Clinical Trial Summary

Rationale: Diabetic neuropathy is one of the most common complications of Diabetes Mellitis (DM). Pain is a common symptom of diabetic neuropathy, affecting 11-34% of patients suffering form DM. The current available medication often provides insufficient pain relief and/or has unacceptable side effects. Spinal cord stimulation (SCS) has been used for over 30 years to treat neuropathic pain. Various small clinical studies have shown a beneficial effect of SCS on pain in PDP.

Objective: This study is a preparation to a RCT to investigate whether SCS is a good indication in patients which suffer from pain with moderate-to-severe PDP in the lower limbs. The main objective of this study is whether SCS leads to sufficient pain relief and to obtain insight into the working mechanism of SCS. The hypothesis is that the effect SCS is most effective in patients without major sensory deficits. Furthermore, practical feasibility of the test procedures described in the study protocol will be examined, including the questionnaires to be filled out by the patient. Also, technical feasibility of SCS will be investigated. Besides the feasibility, the possibility of predicting successful pain relief by SCS by classifying patients according to the Michigan Diabetic Neuropathy Score will be assessed. Furthermore, possible other predictors for successful pain relief by SCS will be defined. Study design: the study is a pilot study in preparation to a RCT to investigate the effect of spinal cord stimulation on pain in moderate-to-severe PDP patients.

Study population: patients suffering from moderate-to-severe PDP in the lower limbs as diagnosed by clinical symptoms and supported by the Michigan Diabetic Neuropathy Score.

Intervention: patients will receive 2 weeks of trial stimulation and best (drug) treatment as usual.

Main study parameters/endpoints: Main study parameter is the pain score as measured by a numeric rating scale (NRS) according to Jensen and a Patient Global Impression of Change for pain measured on a 7-point Likert scale.

Nature and extent of the burden and risks associated with participation, benefit and group relatedness: SCS related risks include: lead migration (14%), lead breakage (7%), implanted pulse generator migration (1%), loss of therapeutic effect, lost or unpleasant paresthesias (12%), infection or wound breakdown (10%), Pain at IPG incision site (12%), IPG pocket fluid collection (5%).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 15
• Est. completion date: July 2010
• Est. primary completion date: July 2010
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Moderate-to-severe PDP in the lower limbs

• The pain intended to treat has been present for more than 12 months

• Previous treatment has been unsuccessful (insufficient pain relief and/or unacceptable side-effects) with drugs from the following drug categories:

• Amitriptyline or an other tricyclic antidepressant and/or

• Pregabalin (Lyrica), Gabapentin (Neurontin) or Carbamazepine and/or

• Duloxetine (Cymbalta) and/or

• Tramadol or strong opioids Patients were treated with 3 drugs from the above mentioned drug categories and followed the treatment algorithm for painful diabetic polyneuropathy according to Jensen. Each drug is tried for 3 weeks and dose is raised once. By insufficient pain relief and/or unacceptable side-effects, the drug treatment was stopped. Patients reached a steady state in medication use and it is not allowed to change the use of medication during the study.

• Mean pain intensity should be 5 or higher measured on a numeric rating scale (NRS), which will be scored 3 times per day during 4 days according to Jensen.

• Patients age is between 18 and 75 years.

Exclusion Criteria:

• The patient has had neuromodulation therapy during the month before the intake

• The patient has ever had neuromodulation

• Neuropathic pain prevalent in the upper limbs (NRS above 3)

• Neuropathy or chronic pain of other origin than diabetes mellitus (NRS above 3)

• Addiction: drugs, alcohol (5E/day) and/or medication

• Drugs: cocaine, heroine, marihuana,

• Alcohol: wine, beer, liquor.

• Medication: benzodiazepines, morphine receptor agonists.

• Insufficient cooperation from the patient (little motivation, understanding or communication)

• Blood clotting disorder

• Immune deficiency (HIV-positive, corticosteroids with a dose equivalent to prednisolone 10 mg, immunosuppressive, etc.)

• Peripheral vascular disease, no palpable peripheral pulsations at the feet (inclusion is possible if pulsations are absent, but ankle/brachial index is between 0.7 and 1.2 in both feet)

• Active foot ulceration

• Life expectancy shorter than 1 year

• Pacemaker

• Local infection or other skin disorders at site of incision

• Psychiatric disorders

• Pregnancy

• Severe cardiac or pulmonary failure (NYHA classification II or higher)

• Unstable blood glucose control (change in HbA1c more than 1,0% (absolute value) in three months prior to inclusion)

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Diabetic Neuropathies
• Polyneuropathies

Intervention

Device:
• spinal cord stimulation
The intervention is spinal cord stimulation and will be used for 2 weeks trial stimulation. After clinical successful pain relief (50% of more pain reduction)a definite spinal cord system will be implanted.

Locations

Country	Name	City	State
Netherlands	Maastricht University Hospital	Maastricht	Limburg

Sponsors (1)

Lead Sponsor	Collaborator
Maastricht University Medical Center

Country where clinical trial is conducted

Netherlands, 

References & Publications (2)

de Vos CC, Rajan V, Steenbergen W, van der Aa HE, Buschman HP. Effect and safety of spinal cord stimulation for treatment of chronic pain caused by diabetic neuropathy. J Diabetes Complications. 2009 Jan-Feb;23(1):40-5. doi: 10.1016/j.jdiacomp.2007.08.002. Epub 2008 Apr 16. — View Citation

Tesfaye S, Watt J, Benbow SJ, Pang KA, Miles J, MacFarlane IA. Electrical spinal-cord stimulation for painful diabetic peripheral neuropathy. Lancet. 1996 Dec 21-28;348(9043):1698-701. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pain intensity measured on a weighted NRS according to Jensen and a PGIC for pain measured on a 7-point Likert scale.		Baseline, 2 weeks after trial stimulation, 3, 6 and 12 months	No
Secondary	The practical- and technical feasibility of the procedures, predicting successful pain relief by SCS by classifying patients according to the MDNS. Define possible other predictors for successful pain relief.		Baseline, 2 weeks after trial stimulation, 3, 6 and 12 months	No