Phase 4 Long COVID Trial, Recruiting NCT06980636 Sponsor: Beijing University of Chinese Medicine Condition: Long COVID
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Phase 4 Long COVID Trial, Recruiting

NCT06980636
Recruiting Phase 4

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 who are between 18 and 75 years old
  • People whose condition meets the specific disease diagnosis criteria set out for this trial (confirm with trial site)
  • People whose condition also meets the traditional Chinese medicine pattern diagnosis criteria set out for this trial (confirm with trial site)
  • People who are willing to give their agreement to take part and sign a consent form

Who may not be able to join:

  • People who currently need, or are expected to need, advanced breathing support such as high-flow oxygen, breathing machines, or a heart-lung bypass machine (ECMO)
  • People with a known history of active liver disease — such as active hepatitis B or C, a specific type of liver scarring (primary biliary cirrhosis), moderate or severe liver failure, or sudden liver failure — or whose blood test results at the start of the trial show certain liver markers above acceptable levels
  • People who are on dialysis, or who have been found in the past 6 months to have moderate to severe kidney disease based on a specific kidney function calculation
  • People who, in the 6 months before the trial, have had moderate to severe heart failure, a stroke, a heart attack, or a coronary artery stent placed; or who have uncontrolled high blood pressure or certain significant heart rhythm abnormalities on an ECG
  • People who had influenza A, influenza B, or another infectious illness in the 3 months before the trial
  • People who have, or have ever had, a serious neurological condition such as epilepsy or seizures, a mental illness, or a family history of mental illness
  • People who are pregnant or breastfeeding, or who have a positive pregnancy test before starting the study medication
  • People who have had a malignant (cancerous) tumour in the 5 years before the trial, or whose cancer is currently active or progressing and may need treatment during the study
  • People who have chronic fatigue syndrome or an autoimmune disease such as rheumatoid arthritis or lupus
  • People who have a known allergy to any ingredient in the study drug
  • People whose overall health condition is considered by the trial doctor to make participation unsuitable
  • People who have taken certain traditional Chinese medicines containing specific herbs — Codonopsis pilosula, Ophiopogon japonicus, Schisandra chinensis, or Astragalus membranaceus — in the 2 weeks before the trial
  • People who are currently taking part in another clinical trial involving a drug or medical device

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 28 July 2026
Phase 4 trials study a drug that has already been approved, monitoring long-term safety and effectiveness in real-world use.

Contact this trial

Phone: 0086 +13466615885

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 4
Sponsor
Beijing University of Chinese Medicine
Registry
ClinicalTrials.gov
Start date
1 December 2025
Est. completion
30 October 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

The degree of improvement in patient fatigue, measured using the Modified Fatigue Impact Scale (MFIS)

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: 28 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