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Completed

NCT Number: NCT04390178

Convalescent Plasma as Treatment for Acute Coronavirus Disease (COVID-19)

There is currently no effective treatment for COVID-19 except best supportive care. The aim is assess the safety, tolerability and efficacy of convalescent plasma for treatment of patients with varying degrees of COVID-19 illness.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Danderyd Hospital

Danderyd, 182 57, Sweden

About this study

Convalescent plasma has been shown to be safe and effective for treatment of several diseases. Preliminary data indicates that it is safe and effective for treatment of COVID-19. However, data is limited to small studies and case series on severely ill patients. The proposed study assesses the safety and efficacy earlier in the course of illness, in slightly less severe patients with the possibility of detecting less severe adverse events and the potential for early treatment to hinder the development of severe disease. Plasma is collected from consenting donors who have recovered from SARS-CoV-2.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age 18 and <81 years
  • Active COVID-19 defined as symptoms + SARS CoV-2 identified from upper or lower airway samples
  • Fever ≥38.5C, admitted to a study hospital, hypoxemia defined as having a peripheral oxygen saturation below 93% (measured by pulse oximetry) and a breathing rate of >20 breaths per minute without supplemental oxygen treatment
  • A negative pregnancy test taken before inclusion and use of an acceptable effective method of contraception until treatment discontinuation if the participant is a woman of childbearing potential
  • Written informed consent after meeting with a study physician and ability and willingness to complete follow up.

Exclusion criteria

  • No matching plasma donor (exact matching in both the ABO system and the Rh system is required)
  • Unavailability of plasma
  • Significant growth of alternative lower airway pathogen such as Streptococcus pneumoniae or Haemophilus influenzae in sputum
  • Disease duration >8 Days
  • Estimated glomerular filtration rate <60 (kidney failure stage III or more)
  • Pregnancy (urinary-hcg), breast feeding,
  • History of severe allergic reactions
  • Inability to give informed consent
  • Significantly compromised immunity.*
  • Compromised immunity includes but is not limited to treatment with major immunosuppressive agents including high dose corticosteroids, anti-tumor necrosis factor (TNF) agents, calcineurin inhibitors, mTOR inhibitors, lymphocyte depleting biological agents, chemotherapeutic anti neoplastic agents. Also patients with advanced HIV/AIDS, severe immunodeficiency such as hypoglobulinemia, decompensated liver cirrhosis and bone marrow transplant the last year will be excluded.

Treatment and study plan

SARS-CoV-2 convalescent plasma

Biological

Treatment with convalescent plasma (180-200ml) from individuals who have recovered from SARS-CoV-2 infection

Primary outcomes

  1. Disease progression

    Time frame: 28 days

    Decrease in progression to requiring non-invasive or invasive ventilation

Secondary outcomes

  1. Adverse events (AE)

    Time frame: The reporting period for AEs starts at inclusion and ends at the final follow-up visit 2 months after inclusion.

    Adverse reactions and serious adverse reactions. The safety of the intervention will be assessed with regard to AEs, baseline medical conditions, and findings from the physical examination and laboratory tests. Possible adverse events will be elicited using a modification and Swedish translation (appendix 6) of Common Terminology Criteria for Adverse Events v5.0 and they will be continuously reported to the sponsor. Adverse events related to convalescent plasma therapy shall be followed to assess reversibility.

  2. Time ro resolution of fever and symptoms

    Time frame: Until discharged from the hospital, up to 2 months

    Measured daily until discharged from the hospital.

  3. Clearance of viraemia

    Time frame: Evaluated daily until discharge, at day 28, and last measurement taken at 6 months of follow-up after inclusion.

    SARS-CoV-2 RNA detection by polymerase chain reaction (PCR) in blood or serum. Blood samples for immunological analyses and serology will be taken daily until discharge, on day 28, and at 6 months.

  4. Inflammatory parameter C-reactive protein (CRP)

    Time frame: Until discharged from the hospital, up to 2 months

    Time to normalization of inflammatory parameter C-reactive protein (CRP). Blood sample for this marker will be taken daily until normalized or discharged from hospital.

  5. Inflammatory parameter white blood cell count

    Time frame: Until discharged from the hospital, up to 2 months

    Time to normalization of inflammatory parameter white blood cell count (WBC). Blood sample for this marker will be taken daily until normalized or discharged from hospital.

  6. Inflammatory parameter haemoglobin (Hb)

    Time frame: Until discharged from the hospital, up to 2 months

    Time to normalization of inflammatory parameter haemoglobin (Hb). Blood sample for this marker will be taken daily until normalized or discharged from hospital.

  7. Inflammatory parameter Pro-calcitonin

    Time frame: Until discharged from the hospital, up to 2 months

    Time to normalization of inflammatory parameter Pro-calcitonin. Blood sample for this marker will be taken daily until normalized or discharged from hospital.

  8. Inflammatory parameter Creatine Kinase

    Time frame: Until discharged from the hospital, up to 2 months

    Time to normalization of inflammatory parameter Creatine Kinase. Blood sample for this marker will be taken daily until normalized or discharged from hospital.

  9. Antibody response to SARS-CoV-2

    Time frame: Evaluated daily until discharge, at day 28, and last measurement taken at 6 months of follow-up after inclusion.

    Change in the antibody response to SARS-CoV-2 as measured in serum. Blood samples for immunological analyses and serology will be taken daily until discharge, on day 28, and at 6 months.

Sponsors and collaborators

Lead sponsor

Joakim Dillner

Other

Collaborators

  • Danderyd Hospital
  • Karolinska Institutet
  • Karolinska University Hospital

Registry information

Official study title

Plasma From Individuals Who Have Recovered From Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection as Treatment for Acute COVID-19 Disease

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
May 15, 2020
Registry last updated
Dec 16, 2021

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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