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Impact of Peripheral Afferent Input on Central Neuropathic Pain

NCT05646810 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2022-12-12

No results posted yet for this study

Summary

The overarching aim of this study is to investigate the contribution of peripheral afferent input to spontaneous and evoked central neuropathic pain after a spinal cord lesion or disease.

Conditions

  • Spinal Cord Injuries
  • Spinal Cord Diseases
  • Syringomyelia

Interventions

DIAGNOSTIC_TEST

Lidocaine (10 mg/ml)

Lidocaine (10 mg/ml) will be injected according to established protocols using ultrasound guidance and an aseptic technique by an experienced anesthesiologist.

DIAGNOSTIC_TEST

Isotonic saline

Isotonic saline will be injected according to established protocols using ultrasound guidance and an aseptic technique by an experienced anesthesiologist.

Sponsors & Collaborators

  • University of Aarhus

    lead OTHER

Principal Investigators

  • Jan Rosner, MD · Danish Pain Research Center, Department of Clinical Medicine, Aarhus University

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-12-01
Primary Completion
2023-09-30
Completion
2023-12-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05646810 on ClinicalTrials.gov