Prednisolone and Vitamin B1/6/12 in Patients With Post-Covid-Syndrome

Post-COVID-19 Syndrome Clinical Trial

— PreVitaCOV  

Official title:

Prednisolone and Vitamin B1, B6, and B12 in Patients With Post-COVID-19-Syndrome (PC19S) - a Randomized Controlled Trial in Primary Care

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05638633
• Other study ID #: F001AM02222_1
• Secondary ID: 2022-001041-20
• Status: Recruiting
• Phase: Phase 3
• Start date: November 11, 2022
• Est. completion date: December 31, 2024

Study information

• Verified date: December 2023
• Source: Wuerzburg University Hospital
• Contact: Andreas Klug
• Phone: 0931-20147803
• Email: Klug_A1[@]ukw.de
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a multicenter, randomized, placebo controlled, double-blind phase III trial with four parallel groups studying studying the feasibility of RCT in primary care as well as the effectiveness of treatment with prednisolone and/or vitamin B1/6/12 for PC19S.

Description:

PC19S affects a considerable portion of patients after an infection with SARS-CoV-2 with a broad range of disabling symptoms. Neurotropic vitamins such as vitamins B1, B6, an B12, and drugs with anti-inflammatory properties such as corticosteroids were suggested to alleviate symptoms. The trial is designed as a two-step approach that will 1. prove the feasibility of recruitment and retention of patients with PC19S in a primary care setting (pilot study, n=100) 2. investigate the effectiveness and safety of the treatment drugs alone and of their combination (confirmatory study, n= 340). The pilot study will be transformed into a confirmatory study if feasibility is given, defined as retention rate of 85% after enrollment of 100 patients. Or on recommendation of the Data Safety and Monitoring Board (DSMB). In addition, blood samples wil be analysed for routine parameters and vitamin B12 derivates as well as cytokines.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 340
• Est. completion date: December 31, 2024
• Est. primary completion date: December 31, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. adult patients (at least 18 years old)

2. history of SARS-CoV-2 infection at least 12 weeks ago (the infection must be documented by either a positive PCR or antibody-Test or be confirmed by the patient's GP)

3. symptoms concerning at least one of the following domains: fatigue, dyspnea, cognition, anxiety, depression

4. above mentioned symptom(s) that developed during or after the SARS-CoV-2 infection, that persist until study inclusion, and that are associated with COVID 19 as assessed by the patients' general practitioner or the local investigator

Exclusion Criteria:

1. acute Coronavirus disease (COVID-19) at baseline visit

2. patients who were treated in the intensive care unit because of COVID-19

3. pregnancy/ breastfeeding

4. diabetes mellitus

5. PC19S symptoms that can be explained by an alternative diagnosis

6. History of severe medical conditions such as

• concomitant acute infectious disease
• gastrointestinal ulcer
• liver disease/liver cirrhosis
• malabsorption or condition after bariatric surgery
• chronic airway disease
• chronic heart failure [New York Heart Association (NYHA) III and IV]
• neurological disorders
• untreated hypothyroidism
• significantly impaired glucuronidation
• immunodeficiency or a chronically weakened immune system
• mental disorders
• active cancer
• any other severe medical conditions that preclude participation as determined by responsible physician

7. current use of

• immunosuppressive drugs
• non-steroidal antiinflammatory drugs (NSAID)
• fluoroquinolones
• anticoagulation
• any other drug that could exhibit clinically relevant interactions with the study medication (as described in Fachinformation Prednisolon STADA®, Predni H Tablinen® Zentiva or Fachinformation Vitamin B komplex Hevert). The decision on the clinical relevance of the interactions is at the discretion of the clinical investigator.

8. systemic treatment with prednisolone for at least 7 days or any parenteral application since the end of the acute phase of COVID-19; treatment with vitamins B1, B6, or B12 in doses equivalent to the dose of the study medi-cation for at least 7 days or any parenteral application since the end of the acute phase of COVID-19; vitamin supplements containing vitamin B1, B6, or B12 should have been ceased at least 4 weeks prior to the inclusion of the study

9. known allergies and contraindications to the intervention drugs

10. need of care and/or peer dependency

11. nursing home residents

12. inability to understand the scope of the study, to follow study procedures and to give informed consent or to attend the study sites

13. participation in another interventional trial at the same time or within the past 3 months before enrolment

14. female patients considering to get pregnant during the first month of the trial and within 1 week after the last dose of study drug(s)

Related Conditions & MeSH terms

• COVID-19
• Post-COVID-19 Syndrome
• Syndrome

Intervention

Drug:
• Prednisolone 20 mg/ 5 mg
Administration of prednisolone 20 mg for 5 days, followed by prednisolone 5 mg for 23 days.
• Vitamin B compound (100mg B1, 50 mg B6, 500 µg B12)
Administration of vitamin B compound for 28 days.
• Placebo for Vitamin B compound
Administration of placebo for vitamin B compound placebo for 28 days.
• Placebo for Prednisolon
Administration of placebo for prednisolone 20 mg for 5 days, followed by placebo for prednisolone 5 mg for 23 days.

Locations

Country	Name	City	State
Germany	Unversity Hospital Schleswig-Holstein	Kiel
Germany	University Hospital Tuebingen	Tuebingen
Germany	University Hospital Wuerzburg	Würzburg	Bavaria

Sponsors (3)

Lead Sponsor	Collaborator
Wuerzburg University Hospital	University Hospital Schleswig-Holstein, University Hospital Tuebingen

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pilot phase: Proportion of participants retained after 28 days	feasibility and acceptance of screening and recruitment in primary care; aim > 85 % retention rate of 100 patients enrolled	4 weeks
Primary	Confirmatory phase: Mean difference in PROMIS Total Score from day 0 to day 28	change in symptom severity to day 28 as assessed by specifically tailored total score based on the patient reported outcome measurement information system (PROMIS)	4 weeks
Secondary	PROMIS total and subscores	Severity of each PC19 symptom domain (patient reported outcome measurement information system (PROMIS))	6 months
Secondary	Measure Yourself Medical Outcome Profile (MYMOP)	Severity of three subjectively chosen PC19 symptoms	6 months
Secondary	Overall assessment of functional status	Severity of PC19 symptom burden	6 months
Secondary	PC19 symptom list	checklist, number of subjectively present symptoms	6 months
Secondary	EQ-5D-5L	Health related quality of life, 5 point rating scale, 0 to 20 points, higher scores indicate worse outcomes	6 months
Secondary	visual analogue scale	Health related quality of life, 0 to 100 points, higher scores indicate a better outcome	6 months
Secondary	PHQ 8	Depression, 4 point rating scale, 0 to 24 points possible, higher scores indicate a worse outcome	6 months
Secondary	Chalder Scale	Fatigue, 4 point rating scale, 0 to 33 points possible, higher values indicate a worse outcome	6 months
Secondary	Numeric rating scale for pain	Pain, 10 point rating scale, higher values indicate a worse outcome	6 months
Secondary	Testbatterie zur Aufmerksamkeitsprüfung (TAP)	cognitive function (Alertness: reaction time, distractibility: omissions and reaction time, divided attention: omissions, visual scanning: omissions and reaction time, flexibility: reaction time and errors)	4 weeks
Secondary	Physical exercise	1minute Sit-to-Stand-Test, number of repetitions, BORG Scale, oxygen-saturation	6 months
Secondary	Use of on-demand medication and change in concomitant medication	intake of on-demand medication, daily drug doses	6 months
Secondary	qualitative assessment of acceptance	qualitative interviews with subgroup sample	6 months
Secondary	feasibility/acceptance	exploratory questionnaire, rating scales and grades	6 months