A Study of the Efficacy of Troxerutin in Preventing Thrombotic Events in COVID-19 Patients

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18+
SponsorWestlake University

About this trial

The goal of this clinical trial is to learn if troxerutin works to prevent thrombotic events in mild or severe COVID-19 patients. It will also learn about the safety of troxerutin. The main questions it aims to answer are:

* Does troxerutin lower the number of thrombotic events in participants? * What medical problems do participants have when taking troxerutin? Researchers will compare troxerutin to a placebo (a look-alike substance that contains no drug) to see if troxerutin works to prevent thrombotic events in COVID-19 patients.

Participants will:

* Take troxerutin or a placebo every day for 7 days. * Visit the clinic at the first, fourth, seventh and 28th days after enrollment for checkups and tests * Keep a diary of their symptoms and the number of times of thrombotic events, bleeding events and type II HIT-related thrombocytopenia

Eligibility criteria

Qualifiers

Respiratory rate ≥30 breaths/min

Severe respiratory distress

Oxygen saturation (SpO₂) ≤90% in room air

Progressive deterioration of clinical symptoms with lung imaging showing significant progression of lesions (>50%) within 24 to 48 hours.

Disqualifiers

Pregnant or lactating women.

Postpartum (within 6 weeks).

Extreme weight (100 kilograms).

Clinical need for heparin therapy.

Trial design

Treatments tested in this trial

  • Troxerutin
  • Placebo
  • placebo + low molecular weight heparin
  • troxerutin + low molecular weight heparin

Treatment groups

80 Participants
are divided into 4 treatment groups

Sponsors and collaborators

Westlake University

Lead sponsor

Shaoxing Central Hospital

Collaborator

Affiliated Hangzhou First People's Hospital, School of Medicine, Westlake University

Collaborator