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Long CovidFASTCOV-PNCT06522750

Periodic Fasting for Treatment of Long Covid in Adults: a Pilot Study

A study testing 7-day ambulatory caloric restriction intervention using the Buchinger-Wilhelmi method in people with Long Covid and Chronic Inflammation, run by University of Luxembourg at 1 site in Luxembourg.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Background: Long COVID, characterized by persistent symptoms following acute COVID-19 infection, has emerged as a significant public health concern. Symptoms range from fatigue, cognitive impairments, to respiratory difficulties, affecting patients\' quality of life. Read more about this study

Who is it for?
Ages 18 to 64 years
Conditions the study is for
Long Covid, Chronic Inflammation
What is being tested?
7-day ambulatory caloric restriction intervention using the Buchinger-Wilhelmi method
Could I receive a placebo?
No, everyone receives an active treatment
How many people
20 participants
Where
1 siteLuxembourg
Study dates
19 Feb 2025to 30 Sep 2025
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 64 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Age 18-64
  • Diagnosis Long Covid Syndrome (post-acute COVID-19 symptoms persisting ≥12 weeks)
  • Normal body Mass Index (18.5 to 25 kg/m2)
  • Marginal Iron status ( PF< 25 ng/ml)
  • Able to communicate in and comprehend English and/or German and/or French language
  • Present written / signed declaration of consent
  • Ability to understand the patient information and willingness to sign the consent form
  • Consent to specimen collection and specimen use

Who cannot join

  • Current underweight condition (body mass index less than 18.5 kg/m2) or weight loss exceeding 3 kg within the last month or 5 kg within the last three months.
  • Existing / current eating disorder within the past five years (e.g., anorexia, bulimia).
  • Psychiatric condition that limits understanding of the examination protocol (unable to consent)
  • Severe internal disease (e.g. kidney deficiency with creatinine > 2mg/dl), chronic inflammatory illness other than LCS
  • Participation in another intervention study.
  • Existing vegan diet or fasting during the last six months
Show all 13Show fewer
  • Pregnancy or breastfeeding status.
  • Presence or suspicion of pre-existing ME/CFS or early autonomous dysfunction
  • Diagnosis of chronic inflammatory bowel diseases, celiac disease or colorectal cancer according to the guidelines of the German Society of Gastroenterology
  • Use of anti-psychotic drugs
  • Antibiotic use during the previous 12 months
  • Start of novel drug therapy
  • Contraindication for additional blood draws (e.g. hemoglobin <10)

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Marta Sanchez, PhD contact

+3524666446555

marta.sanchez@uni.lu

Luxembourg1 site, 1 recruiting
  • Rehaklinik CHNP

    Ettelbruck, L-9012

    Raquel Gómez-Bravo Gómez-Bravo, MD PhD, raquel.gomezbravo@chnp.lu

    Recruiting

Other trials in Luxembourg

About this study

Official title: Pilot Study on the Feasibility of an RCT: Evaluating Periodic Fasting as a Treatment Strategy for Long Covid in Adults

Background:

Long COVID, characterized by persistent symptoms following acute COVID-19 infection, has emerged as a significant public health concern. Symptoms range from fatigue, cognitive impairments, to respiratory difficulties, affecting patients\&#39; quality of life. Dietary interventions, particularly fasting, have historically been used to modulate immune responses and improve health outcomes in various conditions. The Buchinger-Wilhelmi method represents a structured and medically supervised fasting approach. Given the inflammatory nature of long COVID, fasting may offer therapeutic benefits by modulating the immune response, enhancing cellular repair mechanisms, and resetting metabolic processes.

Read more

Objectives:

This clinical trial aims to assess the feasibility of a 7-day ambulatory fasting intervention using the Buchinger-Wilhelmi method on long COVID patients as primary objective. As secondary objectives, the study will investigate the potential beneficial impact of fasting on clinical, biological, and psychological parameters over a period of 4 weeks, offering insights into potential therapeutic avenues for long COVID management.

Study timeline:

The research will span a period of 4 weeks

Study population:

This study aims to recruit around 20 participants, who will all receive a fasting intervention using the Buchinger-Wilhelmi method.

Biological sample and data collection:

Participants will undergo various data and sample collection procedures, including blood draws of up to 90 42 ml per visit, collection of peripheral mononuclear cells, stool samples, and completion of questionnaires in a smartphone-based Application (MyCap).

Sample analysis:

The collected samples will be subjected to a range of analyses, including the assessment of serological markers for routine blood chemistry, evaluation of inflammation markers, and examination of stool samples.

Read the detailed description

Background Long COVID syndrome (LCS) is a heterogeneous clinical condition that develops after acute SARS-CoV-2 infection, affecting at least 10% of patients. LCS is characterized by persistent symptoms lasting longer than 2-3 months following a confirmed SARS-CoV-2 infection. The most disruptive symptoms include fatigue, shortness of breath, pain, depression/anxiety, and cognitive impairment, significantly impacting daily activities, income, and quality of life.

Pathophysiology of LCS

Immunological Dysregulation:

Persistent activation of monocyte populations, including resident and infiltrating macrophages, dendritic cells, and neutrophils, potentially causing tissue damage.

Reservoirs of SARS-CoV-2 may persist, particularly in respiratory and gastrointestinal tracts, contributing to ongoing lymphocyte activation.

Autoimmunity involving T-cells and B-cells has been observed, with cytokines such as interferon gamma, IL-2, IL-4, IL-6, IL-8, IL-10, and IL-17 frequently implicated.

Tissue fibrosis, a consequence of inflammation, is commonly reported.

Vascular Dysfunction and Coagulopathy:

Impaired fibrinolysis and platelet hyperactivation contribute to microclot formation, entrapping pro-inflammatory molecules like IL-6.

Platelet-poor plasma in LCS patients shows high levels of fibrin amyloid microclots, impairing microcirculation and exacerbating immunopathology.

Aberrant immune cell activity increases thrombosis through autoantibodies and NETosis.

Persistent endothelial dysfunction is a common feature, contributing to numerous LCS symptoms.

Gastrointestinal Involvement:

SARS-CoV-2 infection reduces intestinal microbiota diversity, with recovery correlating to reduced LCS risk.

Specific bacterial taxa, such as Escherichia, are associated with severe COVID-19 and LCS.

Functional dyspepsia and irritable bowel syndrome, related to microbial dysbiosis, are common post-COVID conditions.

Gut microbiota influences LCS-related biological functions, particularly psychological symptoms, through modulation of brain chemicals and gut-blood barrier disruption.

Potential of Fasting as a Treatment for LCS Fasting shows promise as a treatment for LCS by modulating the same cellular systems affected by LCS. A recent small study indicated that 92% of LCS patients experienced symptom improvement during long-term fasting, with notable effects on circulating inflammatory molecules, C-reactive protein levels, and dyslipidemia. Fasting can increase beneficial gut microbial genera and alter blood metabolites, potentially disrupting dysfunctional circuits in LCS.

Significance LCS affects over 150 million people worldwide, with more than half experiencing significant work and lifestyle disruptions. Effective, low-cost, and attainable therapeutic options are urgently needed. Medically supervised fasting, particularly intermittent fasting, could be an accessible and safe intervention with minimal physician oversight and low malnutrition risk. Fasting may also prevent other chronic illnesses associated with LCS, such as type 2 diabetes mellitus.

Hypothesis Our primary hypothesis is that ambulatory fasting intervention using the Buchinger-Wilhelmi method is a feasible treatment for LCS. We propose that medically supervised long-term fasting will improve perceived health and quality of life in LCS patients by disrupting inflammatory immuno-metabolic feed-forward loops, thus ameliorating immune and vascular pathologies.

Methodology and Analysis Patient Eligibility

Inclusion Criteria:

Age 18-64 Diagnosis of LCS (post-acute COVID-19 symptoms persisting ≥12 weeks) Normal BMI (18.5 to 25 kg/m²) Marginal iron status (PF < 25 ng/ml) Ability to communicate in and comprehend English, German, or French Written and signed consent Willingness to consent to specimen collection and use

Exclusion Criteria:

BMI < 18.5 kg/m² or significant recent weight loss History of eating disorders within the past five years Severe internal disease or chronic inflammatory illness other than LCS Participation in another intervention study Recent fasting or vegan diet Pregnancy or breastfeeding Existing ME/CFS or early autonomous dysfunction Chronic inflammatory bowel diseases, celiac disease, or colorectal cancer Use of anti-psychotic drugs or recent antibiotic use Contraindication for additional blood draws Start of novel drug therapy Intervention

The primary goal is to perform a single period of periodic fasting (PF) using the Buchinger procedure, involving an initial bowel cleanse followed by a 7-day fasting period. The fasting regimen includes:

Preparation Phase: Three days of relief with reduced food intake, avoiding stimulants.

Fasting Week: A laxative fluid intake on the first day, followed by 7 days of a dietary energy supply of a maximum of 350 kcal per day (vegetable broths and juices), and consumption of calorie-free water or tea.

Support and Guidance: Detailed instructions, face-to-face consultations, and digital application (MyCap) for adherence confirmation via urine ketone measurements.

Sample and Data Collection Sample Size: 20 patients for the pilot study to test feasibility.

Study Outline:

Inclusion visit for risk explanation, medical history, and physical examination.

Daily follow-up via telephone and online appointments during the fasting phase. Questionnaire-based assessment via MyCap Smartphone Application.

Parameters to be Quantified:

Blood samples for safety parameters, metabolites, immune activity indicators, and additional analyses.

Stool samples for microbiome composition and activity. Urine samples for metabolomics. Saliva samples for cortisol measurements. Analysis and Results Interpretation Results will be analyzed descriptively, with means, standard deviations, and graphs summarizing data. Exploratory analysis will identify patterns, trends, or unexpected results. Correlation with improvement in biomedical parameters will be assessed, with a larger study needed for establishing causal links.

Risks Blood Draw: Discomfort, bleeding, swelling, pain, rare nerve damage, or infection at the injection site, and fainting risk.

Periodic Fasting Protocol: Reduction in blood pressure, closely monitored with non-medical interventions if necessary.

Data Collection and Storage Data is collected using REDCap, a secure, web-based software platform, with pseudonymized data stored for at least 10 years post-study. The Principal Investigator ensures compliance with national laws and GDPR.

Regulatory and Ethical Considerations Informed Consent: Participants receive an easily understood Participant Information Sheet and Informed Consent Form, with contact information for study personnel.

Confidentiality and Privacy: Compliance with national laws and GDPR, with pseudonymized data transfer to third parties only with participant consent.

Financing and Insurance: Supported by the Direction de la Santé, CHNP, and the University of Luxembourg.

Conclusion This pilot study aims to test the feasibility of using the Buchinger-Wilhelmi fasting method for treating LCS. If successful, fasting could provide a low-cost, accessible, and effective therapeutic option for LCS sufferers worldwide.

Being tested
7-day ambulatory caloric restriction intervention using the Buchinger-Wilhelmi method
Keywords
long covid, fasting, caloric restriction, chronic inflammation, dysbiosis, mitochondrial dysfunction, thrombosis
Medical subject headings
Post-Acute COVID-19 Syndrome, Fasting, Dysbiosis, Mitochondrial Diseases, Thrombosis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • 7-day ambulatory caloric restriction intervention using the Buchinger-Wilhelmi methodOther

    Buchinger-Wilhelmi method, will be administered in an ambulatory setting under physician guidance. It involves an initial bowel cleanse followed by 7-day fasting period. The initial bowel cleanse will be performed according to the standard procedure commonly used for colonoscopy preparation. During the fasting period, subjects will be provided with a dietary energy supply of a maximum of 350 kcal per day, primarily consisting of vegetable broths as well as fresh vegetable juices. Patients will only be allowed to consume calorie-free and unsweetened water or tea in addition to the prescribed diet.

Study groups in NCT06522750
Study groupRoleWhat they receive
20 participants. Long covid patients.ExperimentalAll patients will undergo a caloric restriction diet for a week.This begins with the intake of a laxative fluid on the first fasting day. This fluid aids in bowel emptying, akin to preparations for a colonoscopy. Detailed instructions on how to use it will be provided along with the laxative, and the study physician or dietary team will discuss dosage and intake with you. The caloric restriction period will last for 7 days and then be broken with the consumption of an apple. Following the breaking of the fast, three build-up days will follow to gradually increase food intake.
Receives: Other: 7-day ambulatory caloric restriction intervention using the Buchinger-Wilhelmi method

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Nutritional protocol

    Patient's level of health and wellbeing from a nutritional point of view

    Measured: 4 weeks

  2. Fatigue assessment Scale (FAS)

    Level of fatigue through three factors (General Fatigue, Physical Fatigue and Concentration/Motivation).

    Measured: 4 weeks

  3. Quality of Life (WHOQOL)

    Quality of Life as an individual's perception of their position in life in the context of the culture and value systems in which they live and in relation to their goals, expectations, standards and concerns.

    Measured: 4 weeks

  4. Functionality (WHODAS 2.0)

    Impact of Long Covid in terms of functioning.

    Measured: 4 weeks

  5. Anxiety (GAD-7)

    Generalized anxiety disorder in the last 2 weeks

    Measured: 4 weeks

  6. Depression (PHQ-9)

    Presence and severity of depressive symptoms

    Measured: 4 weeks

  7. Mood States

    Transient fluctuating moods or affective states

    Measured: 4 weeks

  8. Blood preasure

    Force or pressure of blood on the arteries when the heart is pumping

    Measured: 4 weeks

Secondary outcomes (7)
  1. Urine Metabolomics

    Metabolites in urine

    Measured: 4 weeks

  2. Gut Microbiome

    Microbiota in stool

    Measured: 4 weeks

  3. Stool Metabolomics

    Metabolites in stool

    Measured: 4 weeks

  4. Blood cytokines

    Cytokines using Quanterix technology

    Measured: 4 weeks

  5. Blood Mitochondrial dysfunction

    Mitochondrial cell-free DNA

    Measured: 4 weeks

  6. Blood Epigenetics

    Methylation profiling microarray

    Measured: 4 weeks

  7. Blood test

    Metabolites in blood

    Measured: 4 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Jul 2024
  2. Study start19 Feb 2025
  3. Primary completion30 Jun 2025 (estimated)
  4. Study completion30 Sep 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
20 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06522750
Sponsor's protocol ID
202401/03
Acronym
FASTCOV-P
Status last verified
Mar 2025
First submitted
17 May 2024
Last updated
30 Mar 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing 7-day ambulatory caloric restriction intervention using the Buchinger-Wilhelmi method in people with Long Covid and Chronic Inflammation, run by University of Luxembourg at 1 site in Luxembourg.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 30 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Luxembourg. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Marta Sanchez, PhD (+3524666446555, marta.sanchez@uni.lu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Nutritional protocol (time frame: 4 weeks). The study lists 8 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Mar 2025.

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