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OpenTrials
Completed

NCT Number: NCT04507282

Eosinophil and Anticoagulation in COVID-19 Patients

Despite prophylactic anticoagulant treatments, thrombotic complications may develop in patients with Coronavirus disease 2019 (COVID-19). This study aimed to evaluate anti-Factor Xa levels to determine the anticoagulant activity of low molecular weight heparin (LMWH) in COVID-19 patients.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Bursa Yüksek İhtisas Hastanesi

Yıldırım, 16310, Turkey (Türkiye)

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients older than 18 years, who were diagnosed with COVID-19 and were administered LMWH,
  • agreed to participate in the study were included

Exclusion criteria

  • Patients with previous coagulopathy,
  • continuous indication of anticoagulant therapy (atrial fibrillation (AF), valve disease),
  • glomerular filtration rate (GFR) <30 mL/min or undergoing dialysis, or with known liver dysfunction were excluded from the study.

Treatment and study plan

LMWH

Drug

COVID 19 positive patients anticogulation level, subprophylactic level and prophylactic level

Primary outcomes

  1. subprophylactic anticogulation level

    Time frame: 14 days

    <0.2IU/ml

Sponsors and collaborators

Lead sponsor

Bursa Postgraduate Hospital

Other

Registry information

Official study title

Bursa Yüksek İhtisas Eğitim ve Araştırma Hastanesi

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Aug 11, 2020
Registry last updated
Aug 18, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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