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NCT04399330 Clinical Trial

ME/CFS, Hypermobility and Craniocervical Obstructions

Chronic Fatigue Syndrome Clinical Trial

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04399330
Other study ID # Meret2019
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 1, 2019
Est. completion date September 30, 2019

Study information
Verified date May 2020
Source Bragee Clinics
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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

Recruitment information / eligibility
Status Completed
Enrollment 225
Est. completion date September 30, 2019
Est. primary completion date September 30, 2019
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

Patients at a multidisciplinary specialist clinic accepting to participate

Exclusion Criteria:

none

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Sweden Bragee Clinics Stockholm

Sponsors (2)
Lead Sponsor Collaborator
Bragee Clinics Karolinska Institutet

Country where clinical trial is conducted

Sweden, 

Outcome
Type Measure Description Time frame Safety issue
Primary Prevalence of cervical obstruction and other MRI findings Findings as disc bulging, disc hernias, chiari malformations 1990-2020
Primary Prevalence of hypermobility Measured as Beighton score and other signs of Ehlers Danlos syndrome (EDS) variations 1990-2020
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