Actively Recruiting
Randomized, Double-blind, Placebo-controlled Trial of the Efficacy and Safety of Tianeptine in the Treatment of Covid Fog Symptoms in Patients After COVID-19.
Led by Military Institute od Medicine National Research Institute · Updated on 2023-08-25
140
Participants Needed
1
Research Sites
245 weeks
Total Duration
On this page
Sponsors
M
Military Institute od Medicine National Research Institute
Lead Sponsor
A
ABM Industries
Collaborating Sponsor
AI-Summary
What this Trial Is About
COVID-19 is associated with a high risk of complications from the central nervous system. Syndrome of cognitive disorders- in terms of memory, attention or executive functions among COVID-19 convalescents is often called brain fog (covid fog - CF). CF leads to psychomotor retardation and chronic fatigue syndrome, resulting in poor functioning and low quality of life. CF may affect up to 81% of patients after COVID-19. Prevalence of CF may be even greater among patients with severe forms of COVID-19. In the preliminary assessment authors found that 83% of COVID-19 inpatients had at least mild cognitive impairment. Moreover, SARS-CoV-2 infection is associated with higher incidence of depression and anxiety disorders. CF pathogenesis is not fully understood. There exist no strict diagnostic criteria for it, as well as no therapeutic recommendations. Health care systems of many countries, including Poland, lack therapeutic programs addressed at patients with CF. Tianeptine may be a drug with potentially beneficial effects in CF. Neuroprotective, antidepressive, sleep-improving and anxiolytic properties of tianeptine allow it to choose as a candidate for CF amelioration. There is also data supporting the thesis that patients with CF may benefit from short-term group therapy. It has been proven to improve quality of life, reduce stress, and improve cognitive function in non-MC cognitive disorders. Expected research results: A database will be created from the collected clinical, laboratory and additional data. Statistical models will be created to predict: the duration of disorders, response to therapy, the final result of treatment. Among the markers of CNS damage, those which correlates with the patient's condition will be selected. The study will allow to estimate the prevalence of CF in the population. PET-CT and auditory evoked potentials also will be used to expand knowledge in the field of CF. Based on the existing data, an improvement is expected in all investigated participants as a result of rehabilitation and psychotherapy. Additional improvement is expected in the tianeptine group. Improvement will be defined as: reduction in the severity of anxiety and depression disorders, reduction in the severity of cognitive disorders, improvement in the quality of life. The results will be used to develop a new diagnostic and therapeutic pathway and a comprehensive intervention program in CF.
CONDITIONS
Official Title
Randomized, Double-blind, Placebo-controlled Trial of the Efficacy and Safety of Tianeptine in the Treatment of Covid Fog Symptoms in Patients After COVID-19.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Provided written informed consent to participate
- Age 18 years or older
- Confirmed history of COVID-19 infection by positive SARS-CoV-2 RT-PCR or antigen test
- Patient-reported cognitive decline after COVID-19 infection
- Cognitive dysfunction with Montreal Scale for the Assessment of Cognitive Function (MoCA) score below 26
- Use of effective contraception for women who can bear children
You will not qualify if you...
- Allergy or hypersensitivity to tianeptine or fluorodesoxyglucose (FDG)
- History of stroke or planned brain surgery
- Previously diagnosed organic damage to the central nervous system
- Diagnosed organic mental disorder, bipolar affective disorder, or psychotic disorder
- Current or recent depressive episode requiring antidepressant treatment
- Diagnosed mental retardation
- Bipolar affective disorder in a first-degree relative
- Uncontrolled diabetes mellitus
- Severe kidney failure (eGFR less than 30 ml/min/1.73 m2)
- Severe liver cirrhosis (Child-Pugh class C)
- Claustrophobia
- Chronic diseases significantly worsening prognosis or quality of life
- Active or recent malignancy within 5 years except certain skin and cervical cancers
- Active infections (viral, bacterial, fungal, tuberculous, parasitic)
- Other relevant diseases contraindicating participation
- Positive pregnancy test at screening
- Use of non-selective MAO inhibitors within 14 days prior to screening or mianserin during screening
- Difficulties with peripheral venous cannulation
- History of alcohol, drug, or psychoactive substance abuse or dependence
- Pregnancy, breastfeeding, or planning pregnancy during study
- Participation in another clinical trial
- Lack of compliance with study requirements
AI-Screening
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Trial Site Locations
Total: 1 location
1
Anna Klimkiewicz
Warsaw, Poland
Actively Recruiting
Research Team
A
Anna Klimkiewicz, MD, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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