Mitochondrial Function in Peripheral Blood Mononuclear Cells, Muscle, and Skin of Long COVID Patients
NCT ID: NCT07134673
Last Updated: 2025-08-21
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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NOT_YET_RECRUITING
54 participants
OBSERVATIONAL
2025-10-01
2026-07-31
Brief Summary
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1. To compare the oxygen use between people with long COVID and people who completely recovered after COVID-19, using three techniques that measure the oxygen use in blood cells, on the skin and in the muscle
2. To test how similar these three techniques are in measuring the oxygen used in the three different tissues
Participants will:
* Complete surveys,
* Wear an activity tracker (7 days),
* Undergo several non-invasive tests, and
* Donate a blood sample The study will take place in UZ Brussel hospital and will take 2 study visits, approximately 7 days apart.
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Individuals with long COVID
History of a confirmed or documented SARS-CoV-2 infection and long COVID according to the World Health Organisation's clinical case definition
No interventions assigned to this group
Convalescent individuals
History of a confirmed or documented SARS-CoV-2 infection, complete recovery after the SARS-CoV-2 infection, no history of long COVID according to the World Health Organisation's clinical case definition
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Presence of long COVID symptoms for a minimum of 6 months.
* History of confirmed or documented SARS-CoV-2 infection.
* Adult (≥18 years of age).
* Post-COVID-19 Functional Status Scale grade 2-4, while they had a grade 0 before the SARS-CoV-2 infection.
* History of confirmed or documented SARS-CoV-2 infection.
* Complete recovery after the SARS-CoV-2 infection, no history of long COVID based on the WHO definition;
* Post-COVID-19 Functional Status Scale \[2\] grade 0 both before the infection and currently.
* Adult (≥18 years of age).
Exclusion Criteria
* Treatment with metabolism altering drugs.
* \> 10 standard units of alcohol (10 grams of alcohol/glass) per week.
* Unable to understand oral and written instructions in Dutch, French or English.
* Allergies to medical adhesive bandages.
* Porphyria and other skin conditions aggravated by sunlight.
Convalescent individuals
* Pre-existing chronic non-communicable diseases (e.g. hypertension, chronic respiratory diseases, diabetes).
* Treatment with metabolism altering drugs.
* \> 10 standard units of alcohol (10 grams of alcohol/glass) per week.
* Unable to understand oral and written instructions in Dutch, French or English.
* Allergies to medical adhesive bandages.
* Porphyria and other skin conditions aggravated by sunlight.
18 Years
ALL
Yes
Sponsors
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Universitair Ziekenhuis Brussel
OTHER
Responsible Party
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Elisabeth De Waele
Head of the Department of Clinical Nutrition, Co-director of Vitality Research Group
Principal Investigators
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Elisabeth De Waele, MD. PhD.
Role: PRINCIPAL_INVESTIGATOR
Vitality Research Group, Metabolism and Nutrition, Vrije Universiteit Brussel (VUB), Clinical Nutrition Department, Universitair Ziekenhuis Brussel (UZ Brussel)
Locations
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Laarbeeklaan 101
Jette, Brussels Capital, Belgium
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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G075423N
Identifier Type: OTHER
Identifier Source: secondary_id
EC-2025-071
Identifier Type: -
Identifier Source: org_study_id
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