Pain Phenotyping in Patients with Neuropathic Pain After Spinal Cord Injury

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

The development of neuropathic pain is one of the most debilitating sequels after a spinal cord injury (SCI). The overall aim of this study is to investigate potential underlying pathophysiological mechanisms of neuropathic pain after SCI. The functionality of the nociceptive pathway in humans as well as its plastic changes following SCI will be inferred with sophisticated sensory and pain phenotyping using quantitative sensory testing (i.e., psychophysical measures), objective neurophysiological measures of pain processing and the recording of pain-related autonomic responses (i.e., galvanic skin response, cardiovascular measures and pupil dilation). In addition, the interplay between the somatosensory and autonomic nervous system and its association with the development and maintenance of neuropathic pain after SCI will be investigated.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: t
View:

• Spinal injury cohort - general inclusion criteria:

• Aged between 18-80 years

• Traumatic and non-traumatic etiology

• Para- and tetraplegic SCI

• Complete and incomplete SCI

• SCI with and without neuropathic pain

• Additional inclusion criteria for longitudinal study:

• SCI since less than one month

• Additional inclusion criteria for cross-sectional study:

• SCI since more than one year

• Control cohorts with peripheral neuropathy:

• General inclusion criteria:

• Aged between 18-80 years

• Neurological disorder affecting the peripheral nervous system (i.e., peripheral neuropathy)

• Peripheral neuropathy with or without neuropathic pain

• Additional inclusion criteria for longitudinal study:

• Peripheral neuropathy since less than one month

• Additional inclusion criteria for cross-sectional study:

• Peripheral neuropathy since more than one year

• Control cohorts without neuropathy / healthy volunteers

• General inclusion criteria:

• Aged between 18-80 years

• No medical condition affecting the peripheral and/or central nervous system (e.g., pain, systemic disease, psychological disorder)

Locations
Other Locations
Switzerland
Balgrist University Hospital
RECRUITING
Zurich
Contact Information
Primary
Michèle Hubli, PD Dr.
michele.hubli@balgrist.ch
+41 44 510 72 03
Time Frame
Start Date: 2024-04-17
Estimated Completion Date: 2030-04-30
Participants
Target number of participants: 300
Treatments
Patients with spinal cord injury with neuropathic pain
Patients with spinal cord injury but without neuropathic pain
Patients with peripheral neuropathy
Healthy subjects
Sponsors
Collaborators: Swiss National Science Foundation
Leads: University of Zurich

This content was sourced from clinicaltrials.gov