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NCT07722000Completed

Different Treatment Options Used for Post Covid-19 Syndrome

Evaluation of Different Treatment Options Used for Post Covid-19 Syndrome

Source: ClinicalTrials.gov · Last updated 28 Jul 2026

Brief summary (registry, in English)

This study aimed to assess functioning during the recovery phase post-COVID-19 and to evaluate symptoms prolonging after COVID-19 infection and how to manage these symptoms.

Status (registry)
Completed
Study type
Interventional
Enrollment
90 (actual)
First submitted
19 Jul 2026
Start date
1 Feb 2021
Primary completion date
1 Dec 2023
Lead sponsor
Beni-Suef University
NCT number
NCT07722000

What you commit to

  • Study type: Interventional
  • Participants enrolled: 90
  • From 1 Feb 2021 to the primary completion date, 1 Dec 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients with pre-existing neurological disorders that could affect cognitive function or fatigue assessment, including dementia, Alzheimer's disease, Parkinson's disease, multiple sclerosis, epilepsy, or prior cerebrovascular stroke, patients with diagnosed psychiatric disorders such as major depressive disorder, bipolar disorder, schizophrenia, or anxiety disorders requiring ongoing pharmacological treatment.
  • Patients with malignancy or receiving chemotherapy, radiotherapy, or immunosuppressive therapy during the study period.
  • Patients with chronic fatigue syndrome, fibromyalgia, or other pre-existing fatigue-related disorders diagnosed prior to SARS-CoV-2 infection.

Other illness

  • Patients with other non-COVID-related chronic illnesses that could interfere with the assessment of post-viral symptoms.
  • Patients with uncontrolled endocrine disorders, particularly uncontrolled diabetes mellitus or thyroid dysfunction.
  • Patients with known hypersensitivity or contraindications to Ginkgo biloba or piracetam.

Other

  • Patients with substance abuse or alcohol dependence, pregnant or lactating women.
  • Patients with poor adherence to treatment or anticipated inability to complete follow-up visits.

Who the study is looking for

  • Patients aged from 18 to 70 years.
  • Both sexes.
  • Positive diagnosis of COVID-19 within the last 3 months in relation to the time of assessment (COVID-19 diagnosis had been previously confirmed by RT-PCR nasal swab testing as part of routine clinical evaluation before enrollment into the study).

Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Beni Suef University
Coordinator of this site? Confirm its status
Banī SuwayfEgyptUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.