Intrathecal Baclofen (ITB) Bolus on Neuropathic Pain (NP). Preliminary Study. (ITB)

Effect of Intrathecal Baclofen (ITB) Bolus on Neuropathic Pain (NP) in Spinal Cord Injury (SCI) Patients. Preliminary Study.

Hypothesis:

ITB bolus can have antinociceptive effect on neuropathic pain in spinal cord injury patients, which could depend on the subtype of pain, or on the lesion level, cervical or thoracic spinal cord injury.

Objective:

To study the effect of intrathecal baclofen bolus on neuropathic pain in patients with spinal cord injury at cervico-dorsal level.

Primary Endpoint:

Effect of intrathecal baclofen bolus in neuropathic pain (measured using the Neuropathic Pain Inventory Scale, the Brief Pain Inventory and the Numerical Rating Scale) in spinal cord injury at cervico-dorsal level.

Secondary Endpoints:

1. Spasticity and spasms (measured using the Modified Ashworth Scale and the Visual Analogue Scale and Penn Spasm Frequency Scale).
2. Neurophysiological examination (warm perception threshold, heat pain perception threshold, evoked pain perception and contact heat evoked potentials).

Study Overview

• Status: Completed
• Conditions: Neuropathic Pain
• Intervention / Treatment: Drug: Intrathecal baclofen bolus; Other: Placebo

Detailed Description

The study will be a randomized, double-blind (patients and who will realize the clinical and neurophysiologic evaluation), placebo-controlled trial. We will recruit 10-12 patients with SCI with complete or incomplete lesion at cervical or thoracic level to be randomly distributed in two study groups: ITB bolus group and a placebo group.

In 6-8 months, we will administer an intrathecal baclofen bolus of 50 µg (1ml) in 5-6 SCI patients or 1ml of physiologic serum subcutaneously in the other 5-6 SCI patients.

Before the intrathecal baclofen or placebo bolus is administered, patients will be evaluated for neuropathic pain, using the Neuropathic Pain Inventory Scale, Brief Pain Inventory and Numerical Rating Scale. Spasticity and spasms will also be measured by the Modified Ashworth Scale, the Visual Analogue Scale and the Penn Spasm. After that, patients will also undergo, early in the morning when the intrathecal baclofen or placebo bolus will be administered, a neurophysiology assessment (warm perception threshold, heat pain perception threshold, evoked pain perception and contact heat evoked potentials).

After the neurophysiological evaluation, patients will receive an intrathecal baclofen bolus of 50 µg or placebo (randomization). After the intrathecal baclofen or placebo injection, a clinical and neurophysiological examination, of neuropathic pain and spasticity and spasms, will be repeated at 1, 2 and 4 hours after the bolus administration. Moreover, Kumru et al. (2013) reported that the 50 µg intrathecal baclofen bolus reduced the pain perception threshold and evoked acute pain perception in patients with SCI.

During all evaluation period, the patients continue with their analgesic, antispastic and/or any other stable medication.

• Study Type: Interventional
• Enrollment (Actual): 12
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Spain
  • Barcelona
    • Badalona, Barcelona, Spain, 08916
      • Institut Guttmann

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 16 years to 68 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Age between 18-70 years and at least one year since the spinal cord injury.
• Aetiology: stable SCI from traumatic or medical origin.
• Patients with chronic refractory neuropathic pain and with spinal cord injury, both complete and incomplete, at the cervico-thoracic level.
• Severity of pain equal or greater than 4 in the Numerical Rating Scale.
• With spasticity (MAS>=).
• Stable analgesic, antispastic and any other medication.

Exclusion Criteria:

• Patients who do not give patient inform consent.
• Contraindication for baclofen or intrathecal injection.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Triple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: intrathecal baclofen bolus; In ITB bolus group: An intrathecal baclofen bolus injection of 50 µg (1ml) will be injected at L3/L4 level. A 50 µg.	Drug: Intrathecal baclofen bolus; An intrathecal baclofen bolus injection of 50 µg (1ml) will be injected at L3/L4 level.; Other Names: ITB bolus
Placebo Comparator: placebo; In the placebo group: 1 ml of physiological saline (isotonic saline) will be injected subcutaneously at L3/L4 level simulating	Other: Placebo; 1 ml of physiological saline (isotonic saline) will be injected subcutaneously at L3/L4 level simulating; Other Names: physiological saline

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Neuropathic Pain Inventory Scale (NPIS)	a self-questionnaire specifically designed to evaluate the different symptoms of neuropathic pain and includes 10 descriptors that allow discrimination and quantification of five distinct clinically relevant dimensions of neuropathic pain syndromes and that are sensitive to treatment	Change from baseline in neuropathic pain at 4hours

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Modified Ashworth Scale (MAS)	is to measure spasticity in patients who have lesions of the central nervous system or neurological disorders.	Change from baseline in spasticity at 1, 2 and 4hours
Modified Penn Spasm Frequency Scale	2 component self-report measure of the frequency of reported muscle spasms which is commonly used to quantify spasticity.	Change from baseline in spasticity at 4hours
Visual Analogue Scale (VAS) for spasticity	Consists 10cm line for patient self-reporting of spasticity last 24hours	Change from baseline in spasticity at 4 hours
warm and heat pain perception threshold	it is quantitative sensory perception test for warm perception threshold and heat pain perception threshold	Change from baseline in warm and pain perception at 4hours
evoked pain perception	it is quantitative sensory perception test for acute induced pain perception measurement	Change from baseline in evoked acute pain perception at 4hours
contact heat evoked potentials.	It is an evoked potential induced with heat painful stimulus	Change from baseline in evoked potential with heat pain at 4hours
Brief Pain Inventory (BPI)	The BPI allows patients to rate the severity of their pain and the degree to which their pain interferes with common dimensions of feeling and function.	Change from baseline in pain at 4hours
Numerical Rating Scale (NRS) for neuropathic pain	Varies between 0-10 point (no pain- more severe pain) for patient self-reporting of pain for actual pain	Change from baseline in pain at 4hours

Collaborators and Investigators

• Sponsor: Institut Guttmann
• Collaborators: Medtronic
• Investigators: Principal Investigator: Hatice Kumru, MD PhD, Neurologist

Study record dates

Study Major Dates

• Study Start: December 1, 2014
• Primary Completion (Actual): August 1, 2017
• Study Completion (Actual): August 1, 2017

Study Registration Dates

• First Submitted: February 25, 2016
• First Submitted That Met QC Criteria: March 10, 2016
• First Posted (Estimate): March 11, 2016

Study Record Updates

• Last Update Posted (Actual): August 8, 2019
• Last Update Submitted That Met QC Criteria: August 6, 2019
• Last Verified: August 1, 2019

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Nervous System Diseases; Pain; Neurologic Manifestations; Neuromuscular Diseases; Peripheral Nervous System Diseases; Neuralgia; Physiological Effects of Drugs; Neurotransmitter Agents; Molecular Mechanisms of Pharmacological Action; Peripheral Nervous System Agents; GABA Agents; Neuromuscular Agents; Muscle Relaxants, Central; GABA Agonists; GABA-B Receptor Agonists; Baclofen
• Other Study ID Numbers: 2014187

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No