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Structural and Functional Brain Reorganization in Neuropathic Pain: Basal State of Local Cerebral Blood Flow and Functional Connectivity

Structural and Functional Brain Reorganization in Neuropathic Pain: Basal State of Local Cerebral Blood Flow and Functional Connectivity

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02858466
Acronym
CONNECT
Enrollment
68
Registered
2016-08-08
Start date
2016-03-25
Completion date
2019-03-22
Last updated
2020-09-28

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

Conditions

Neuropathic Pain

Brief summary

Neuropathic pain is a medical condition involving allodynia (painful perceptions in response to stimuli that normally are not) and spontaneous pain (occurring at rest, without stimulation). This pain is secondary to nervous system injury affecting the sensory system. The lesion is either at the nerve endings of the spinal cord or brain. It induces a loss of sensitivity and likely reorganization of brain activity that are causing pain and which are the subject of this study. Previous studies in functional neuroimaging has focused on brain areas activated during allodynic stimuli compared to non-painful stimuli. The abnormalities have been reported, but it was not possible to conclude formally. The authors failed to assess the part of the effect of the loss of sensory afferents (deafferentation) and the basal brain function. Indeed, the operation without any sensory stimulation is not known yet is the initial level of activity which is the benchmark for studying brain function during stimulation. The objective of this study is to understand what are the cortical systems of allodynic dysfunctional in patients compared with controls at baseline.

Interventions

RADIATIONMRI scan

Sponsors

Centre Hospitalier Universitaire de Saint Etienne
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

for patients : * major * with nervous pain : chronic or peripheric * treatment not stable opioid since one week * signed consent Inclusion Criteria for witnesses : * major * without chronic pain * signed consent

Exclusion criteria

for 2 groups : * severe psychiatric history * presence of an active nervous lesion * subject with morphine treatment * contraindication to MRI scan

Design outcomes

Primary

MeasureTime frameDescription
cerebral blood flowat baselinequantified with MRI scan

Secondary

MeasureTime frameDescription
rate of grey matterat baselinedifference between groups
structure of the networksat baselineDetermine if structure of the networks is different between patients and controls. Measured with MRI scan.
connection of the networksat baselineDetermine if connection of the networks is different between patients and controls. Measured with MRI scan.
cortical lossat baselineAssess the cortical loss of the patient group compared to controls. Measured with MRI scan.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026