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Recruiting NCT06224959

Migraine and Neuropathic Pain in Osteoarthritis

Observational Osteoarthritis Migraine Neuropathic Pain

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Osteoarthritis, Migraine, Neuropathic Pain. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Prevalence of Migraine and Neuropathic Pain in Osteoarthritis: Multicenter, Multidisciplinary, Cross-sectional Epidemiological Study.

Overview

The goal of this observational study is to estimate the frequency of neuropathic pain and migraines in a group of patients with osteoarthritis of the knees, hips, hands, spine or other joints. In addition to their usual care for osteoarthritis, participants will complete questionnaires to define migraine and neuropathic pain.

Detailed description

This study will be proposed to patients with osteoarthritis who come for their routine consultation. If the patient has no abjection to taking part in the study, the doctor will give them the questionnaires to fill in. The questionnaires are about: perception of pain , depression and anxiety, how patients manage their disease emotionally, migraine, neuropathic pain, functional ability, osteoarthritis assessment.

Primary outcome measures

  • the presence of neuropathic pain in patients [Time frame: 10 minutes]
  • the presence of migraine in patients [Time frame: 10 minutes]
Secondary outcome measures (3)
  • the presence of anxiety and depression symptoms in patients [Time frame: 10 minutes]
  • measure the level of catastrophizing thoughts related to pain in patients [Time frame: 10 minutes]
  • Impact of headhache in patients [Time frame: 10 minutes]

Eligibility criteria

Inclusion criteria

  • patients over 18 years old
  • patients with articular or/and spinal osteoarthritis
  • affiliation to a social security system.
  • able to read and understand french

Exclusion criteria

  • patients who refuse to participate in the study
  • patients unable to complete self-questionnaires
  • minors or adults under the protection of the law or under the protection of justice

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Other

Study locations

France · 1 center
  • CHU Clermont-Ferrand — Clermont-Ferrand

Identifiers

NCT: NCT06224959 · RNI 2023 MATHIEU · 2023-A00093-42

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗