Phase 2 Long COVID Trial, Recruiting NCT06012552 Sponsor: Military Institute od Medicine National Research Institute Condition: Long COVID
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Phase 2 Long COVID Trial, Recruiting

NCT06012552
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People aged 18 or older.
  • People who have had a confirmed COVID-19 infection, shown by a positive PCR or antigen test.
  • People who feel their memory or thinking has gotten worse since having COVID-19, as reported at the screening visit.
  • People who show signs of cognitive (thinking or memory) difficulties at screening, based on a specific memory and thinking test called the MoCA, with a score below 26.
  • Women who could become pregnant must be using effective contraception.
  • People who provide written consent to take part in the trial.

Who may not be able to join:

  • People with a known allergy or sensitivity to the study drug tianeptine.
  • People with a known allergy or sensitivity to a substance called fluorodeoxyglucose (FDG), which is used in a type of brain scan.
  • People with a history of significant drug or substance allergies that the trial doctor considers a reason not to participate.
  • People who have had a stroke.
  • People who have previously had brain surgery, or who have brain surgery planned during the study period.
  • People with a previously diagnosed condition causing physical damage to the brain or nervous system.
  • People diagnosed with an organic mental disorder (a mental health condition caused by a physical brain condition).
  • People diagnosed with bipolar disorder.
  • People diagnosed with a psychotic disorder.
  • People with a history of a depressive episode, including one identified at the time of screening, that requires antidepressant medication.
  • People diagnosed with an intellectual disability (previously called mental retardation).
  • People who have a parent, sibling, or child diagnosed with bipolar disorder.
  • People with uncontrolled diabetes.
  • People with severe kidney disease, where kidney function (eGFR) is below 30 ml/min/1.73m².
  • People with severe liver cirrhosis (the most advanced stage, known as Child-Pugh class C).
  • People with claustrophobia (fear of enclosed spaces), as the trial involves scanning equipment.
  • People with serious ongoing illnesses that, in the trial doctor's opinion, could significantly affect their health outcomes or ability to participate.
  • People with an active cancer diagnosis or a cancer diagnosis within the past 5 years, except for certain treated skin cancers or cervical cancer in situ where full treatment has been completed.
  • People with an active infection of any kind (viral, bacterial, fungal, tuberculosis, or parasitic).
  • People with other medical conditions that, in the trial doctor's opinion, make participation unsuitable.
  • Women of childbearing potential who have a positive pregnancy test at screening or the first visit.
  • People who have taken certain medications recently, specifically non-selective MAO inhibitor drugs within 14 days before screening, or mianserin during the screening period.
  • People who have significant difficulty with having a needle or cannula inserted into a vein.
  • People with a history of alcohol, drug, or psychoactive substance misuse or dependence.
  • People who are pregnant, or planning to become pregnant during the study.
  • People who are breastfeeding, or planning to breastfeed during the study.
  • People currently taking part in another clinical trial.
  • People who, in the trial doctor's opinion, are unlikely to follow the trial requirements.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 27 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: +48695723984

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Military Institute od Medicine National Research Institute
Registry
ClinicalTrials.gov
Start date
17 February 2023
Est. completion
30 April 2027

Where this trial is recruiting

🇵🇱 Poland

Primary endpoints

Improvement in covid fog symptoms

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov