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OpenTrials
Completed

NCT Number: NCT04399330

ME/CFS, Hypermobility and Craniocervical Obstructions

A retrospective study on clinical and radiological findings in ME/CFS

Completed

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Key information

Conditions

Chronic Fatigue Syndrome Chronic Disease Disease Attributes Encephalomyelitis Fatigue Syndrome, Chronic Muscular Diseases Musculoskeletal Diseases Nervous System Diseases Neuroinflammatory Diseases Neuromuscular Diseases Pathologic Processes Pathological Conditions, Signs and Symptoms

Sex eligibility

All sexes

Study type

Observational

Primary location

Bragee Clinics

Stockholm, 11526, Sweden

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Patients at a multidisciplinary specialist clinic accepting to participate

Exclusion criteria

none

Treatment and study plan

Primary outcomes

  1. Prevalence of cervical obstruction and other MRI findings

    Time frame: 1990-2020

    Findings as disc bulging, disc hernias, chiari malformations

  2. Prevalence of hypermobility

    Time frame: 1990-2020

    Measured as Beighton score and other signs of Ehlers Danlos syndrome (EDS) variations

Sponsors and collaborators

Lead sponsor

Bragee Clinics

Other

Collaborators

  • Karolinska Institutet

Registry information

Official study title

Hypermobility and Obstructions in the Craniocervical Region Among Patients With Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)

Important dates

Study start
2019
Primary completion
2019
Study completion
2019
First posted
May 22, 2020
Registry last updated
May 26, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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