GeNeup: Exploring the Genetics of Neuropathic Pain

Sponsor
Oslo University Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT03862365
Collaborator
Haukeland University Hospital (Other), Helse Stavanger HF (Other), St. Olavs Hospital (Other), University Hospital of North Norway (Other), University of Oxford (Other), Danish Pain Research Center (Other), Oslo Metropolitan University (Other)
5,000
5
113
1000
8.9

Study Details

Study Description

Brief Summary

In the present study the investigators will search for new genetic variants relevant for the development of neuropathic pain.

Condition or Disease Intervention/Treatment Phase
  • Genetic: Nerve conduction Studies

Detailed Description

Neuropathic pain is defined as "pain caused by a lesion or disease of the somatosensory nervous system". Neuropathic pain is a huge health problem worldwide, with an estimated prevalence of 7-8 % in the general population. In the present study the investigators will search for new genetic variants relevant for the development of this type of pain.

Peripheral nerve lesions only progress to neuropathic pain in some patients, yet is not completely understood why or how. Genetic studies of patients with rare neuropathic disorders have been important for elucidating novel molecular mechanisms of neuropathic pain, and new drugs for neuropathic pain are now being developed based on these findings. By using genetic association studies, one may identify new genetic variants which may help to identify key molecular mechanisms for a larger group of patients with neuropathic pain.

This project will use existing population-based cohorts, as well as establish a specific registry and biobank for patients with neuropathy in order to address these specific needs. This will allow the investigators to identify a large number of individuals with probable neuropathic pain and individuals with pain-free peripheral neuropathy (disease controls). International collaboration will contribute to study a large group of patients, which will be important in order to reach the project's goals. The results from the project are expected to increase current knowledge on the mechanisms of neuropathic pain, opening up new opportunities for innovative and improved treatments.

Dissemination of results will be organized in close collaboration with patient representatives, and will be done regularly throughout the course of the project. The will focus both on internal dissemination to the participating hospitals, and external dissemination through participation in conferences, submissions to scientific journals and by publishing patient-friendly information booklets and proactively informing media outlets and patient organizations.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
5000 participants
Observational Model:
Case-Control
Time Perspective:
Cross-Sectional
Official Title:
Exploring the Genetics of Neuropathic Pain
Actual Study Start Date :
Aug 1, 2018
Anticipated Primary Completion Date :
Jan 1, 2027
Anticipated Study Completion Date :
Dec 31, 2027

Arms and Interventions

Arm Intervention/Treatment
Polyneuropathy with pain

Clinical and diagnostic test evaluation for the establishment of polyneuropathy with pain.

Genetic: Nerve conduction Studies
Patients will be genotyped for comparison of patients With and without pain, With different clinical subgroups as mentioned.
Other Names:
  • Genetical analysis
  • Polyneuropathy without pain

    Clinical and diagnostic test evaluation for the establishment of polyneuropathy without pain.

    Genetic: Nerve conduction Studies
    Patients will be genotyped for comparison of patients With and without pain, With different clinical subgroups as mentioned.
    Other Names:
  • Genetical analysis
  • Diabetic polyneuropathy with pain

    Clinical and diagnostic test evaluation for the establishment of diabetic polyneuropathy with pain.

    Genetic: Nerve conduction Studies
    Patients will be genotyped for comparison of patients With and without pain, With different clinical subgroups as mentioned.
    Other Names:
  • Genetical analysis
  • Diabetic polyneuropathy without pain

    Clinical and diagnostic test evaluation for the establishment of diabetic polyneuropathy without pain.

    Genetic: Nerve conduction Studies
    Patients will be genotyped for comparison of patients With and without pain, With different clinical subgroups as mentioned.
    Other Names:
  • Genetical analysis
  • Carpal tunnel syndrome with pain

    Clinical and diagnostic test evaluation for the establishment of carpal tunnel syndrome with pain.

    Genetic: Nerve conduction Studies
    Patients will be genotyped for comparison of patients With and without pain, With different clinical subgroups as mentioned.
    Other Names:
  • Genetical analysis
  • Carpal tunnel syndrome without pain

    Clinical and diagnostic test evaluation for the establishment of carpal tunnel syndrome without pain.

    Genetic: Nerve conduction Studies
    Patients will be genotyped for comparison of patients With and without pain, With different clinical subgroups as mentioned.
    Other Names:
  • Genetical analysis
  • Outcome Measures

    Primary Outcome Measures

    1. Genetic variants associated with neuropathic pain. [Baseline]

      Relevant genotypes will be found using genome-wide association study (GWAS) methodology, ie. with no assumptions regarding which genetic variants that may be relevant (no hypotheses regarding specific variants). This is going to be conducted by using array genotyping (SNPs) in order to identify genetic variants that might be associated with neuropathic pain. Genetic variants will be defined and named according to standard practice, without any room for local or study specific adaptations.

    2. Phenotype; neuropathic pain yes/no [Baseline]

      Patients will be divided in two groups; neuropathy With pain (= neuropathic pain) and neuropathy without pain. For definition of neuropathic pain, the Neupsig guidelines (Finnerup et al, Pain 2016) will be used.It is estimated that about 600 patients will be included yearly for this purpose

    3. Phenotype; subgroup analysis of patients with neuropathic pain based on grading of pain [Baseline]

      Patients with neuropathic pain will be further subdivided in groups based on pain reports. Pain will be graded using validated questionnaires. The "Brief Pain Inventory-BPI" (Cleeland et al, 1994) questionnaire will be used as primary resource for pain grading, on a scale from 0 to 10 (0: no pain, 1-3: mild pain, 4-10: strong pain).

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. The patient is between 18 and 70 years old.

    2. The patient has consented.

    3. The patient is referred for evaluation of possible distal symmetric polyneuropathy (DSPN).

    4. The patient has filled out the questionnaires.

    Exclusion Criteria:
    1. The patient is too sick to participate (eg. bedridden, fever).

    2. The patient is unable to consent (eg. dementia, speech problems, psychiatric disorder).

    3. Inflammatory acute polyneuropathy.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Haukeland University Hospital Bergen Norway 5021
    2 Oslo University Hospital Oslo Norway 0450
    3 Helse Stavanger HF Stavanger Norway 4011
    4 University Hospital of North Norway Tromsø Norway 9019
    5 St. Olavs Hospital Trondheim Norway 7030

    Sponsors and Collaborators

    • Oslo University Hospital
    • Haukeland University Hospital
    • Helse Stavanger HF
    • St. Olavs Hospital
    • University Hospital of North Norway
    • University of Oxford
    • Danish Pain Research Center
    • Oslo Metropolitan University

    Investigators

    • Study Chair: John Anker Zwart, M.D., Oslo University Hospital
    • Principal Investigator: David Benett, M.D., University of Oxford
    • Principal Investigator: Ina Hjelland, M.D., Haukeland University Hospital
    • Principal Investigator: Margreth Grotle, Pr., Oslo Metropolitan University
    • Principal Investigator: Marie Bu Kvaløy, M.D., Helse Stavanger HF
    • Principal Investigator: Trond Sand, M.D., St. Olavs Hospital
    • Principal Investigator: Sissel Løseth, M.D., University of North Norway
    • Principal Investigator: Troels Jensen, M.D., Danish pain research senter

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Kristian Bernhard Nilsen, Senior Consultant, phd, Oslo University Hospital
    ClinicalTrials.gov Identifier:
    NCT03862365
    Other Study ID Numbers:
    • 2017/1593
    First Posted:
    Mar 5, 2019
    Last Update Posted:
    Sep 14, 2021
    Last Verified:
    Sep 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Kristian Bernhard Nilsen, Senior Consultant, phd, Oslo University Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 14, 2021