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The effect of Plasmapheresis in the treatment of patients with COVID-19

Study of the therapeutic role of plasmapheresis in patients with COVID-19 and its effect on serum levels of inflammatory factors

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200611047735N2
Enrollment
45
Registered
2021-02-13
Start date
2020-10-22
Completion date
Unknown
Last updated
2021-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COVID-19. COVID-19

Interventions

Intervention group: Plasmapheresis will be performed in 3 sessions at intervals of 24 to 36 hours based on the daily evaluation of the patient in the dialysis ward of Shahid Mohammadi Hospital in Band

Sponsors

Bandare-abbas University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: COVID-19 patients with positive Realtime PCR test for COVID-19 tachypnea> Respiratory Rate 30 per minute and dyspnea, Oxygen saturation lower than 88% and fraction of inspired oxygen/ PaO2 ratio lower to equal 300, and increased lung involvement by more than 50% on CT scan. Patient with symptoms of respiratory failure, patient in need or under mechanical ventilation, patient with multiple organ failure and patient with shock symptoms Presence of two positive inflammatory markers including: Ferritin greater than 1000 or CRP above 50 mg/dl or ' ' +++ ' ' or Lactate dehydrogenase greater than 1000 Lack of proper response to antiviral and corticosteroid therapy and hypoxia during hospitalization

Exclusion criteria

Exclusion criteria: Low blood pressure lower than normal range, which causes a further decrease in blood pressure during plasmapheresis. Coagulation disorders that cause bleeding during plasmapheresis. Decreased blood platelets below the normal range, which may increase bleeding during plasmapheresis.

Design outcomes

Primary

MeasureTime frame
Serum IL-6 levels. Timepoint: Before plasmapheresis and after the last stage of plasmapheresis. Method of measurement: ELISA technique.;Serum IL-1ß levels. Timepoint: Before plasmapheresis and after the last stage of plasmapheresis. Method of measurement: ELISA technique.;Serum TNF-a levels. Timepoint: Before plasmapheresis and after the last stage of plasmapheresis. Method of measurement: ELISA technique.;Serum IFN-? levels. Timepoint: Before plasmapheresis and after the last stage of plasmapheresis. Method of measurement: ELISA technique.;Clinical manifestation. Timepoint: Before plasmapheresis and after the last stage of plasmapheresis. Method of measurement: Clinical examination and completion of a questionnaire.;Inflammatory factors of peripheral blood. Timepoint: Before plasmapheresis and after the last stage of plasmapheresis. Method of measurement: Peripheral blood test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehdi Hassani Azad

Bandare-abbas University of Medical Sciences

mehdi.hassaniazad@gmail.com+98 76 3333 7192

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026