POTS-CFS Study: Orthostatic Intolerance in the Context of Pediatric ME/CFS
NCT ID: NCT06054958
Last Updated: 2023-09-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
40 participants
OBSERVATIONAL
2021-12-06
2022-11-22
Brief Summary
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Detailed Description
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This pilot-case-control study study aimed at characterizing OI in adolescents aged 14-17 years with ME/CFS and age-adapted HC, comparing the results with other clinical features of both such as exertion intolerance, fatigue, and health-related quality of life, and suggesting a standardized tool for diagnostics.
ME/CFS was diagnosed according to the Clinical Canadian Criteria (CCC 2003), criteria of the former Institute of Medicine (IOM 2015), the diagnostic work sheet developed by Rowe 2017, and/or the pediatric case suggested by Jason 2006. Questionnaires were used to evaluate symptoms (e.g. post-exertional malaise, fatigue, anxiety, depression), and health-related quality of life. A standardized specific interview was performed to assess the medical history of OI (HOI). Heart rate (HR) and blood pressure were evaluated every minute during a passive 10-min standing test (NASA lean test) in the morning with empty stomach and without morning medication.
Data were evaluated according to the PoTS criteria defined in 2019 at the National Institutes of Health Expert Consensus Meeting and by the International Classification of Diseases (ICD-11) (8D89.2). Frequency and type of OI, including PoTS, were examined in both groups and outcomes compared to parameters from questionnaires. Based on the results, novel standards for OI diagnostics were suggested.
Conditions
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Study Design
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CASE_CONTROL
CROSS_SECTIONAL
Study Groups
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ME/CFS
ME/CFS: adolescents aged 14-17 years, fulfilling diagnostic criteria for ME/CFS according to Rowe e 2017, Jason 2006, CCC 2003, and/ or IOM 2015 at the time of recruitment.
Methods: Semi-structured interview, questionnaires, passive 10-minute standing test (NASA lean test), blood sampling.
No interventions assigned to this group
Healthy Controls (HC)
HC: adolescents aged 14-17, clinically healthy without any known underlying disease and with no prescription drugs (except contraception).
Methods: Semi-structured interview, questionnaires, passive 10-minute standing test (NASA lean test), blood sampling.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
\- ME/CFS diagnosed by the indicated clinical criteria
2. Healthy Controls
* clinically healthy
* no known underlying disease
* no prescription medication (except contraception)
Exclusion Criteria
* pregnancy
* breastfeeding.
14 Years
17 Years
ALL
Yes
Sponsors
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University Hospital, Aachen
OTHER
Technical University of Munich
OTHER
Responsible Party
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Locations
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MRI Chronic Fatigue Center for Young People (MCFC) Children's Hospital, Technical University of Munich & Munich Municipal Hospital Munich
Munich, Bavaria, Germany
Countries
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Related Links
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Related Info
Related Info
Other Identifiers
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POTS-CFS
Identifier Type: -
Identifier Source: org_study_id
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