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Hemoperfusion effect in treatment of patients with COVID-19

Evaluation of Hemoperfusion effect in treatment of patients with COVID-19 hospitalized in intensive care unit, Randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110425006280N12
Enrollment
20
Registered
2021-08-14
Start date
2021-08-23
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

The effect of Hemoperfusion in the treatment of covid-19 disease. COVID-19, virus identified

Interventions

Intervention 1: Intervention group includes 10 patients who enter the study after obtaining the informed consent of the patient or her companion and receive the standard COVID-19 treatment regimen alo

Sponsors

Vice President of Research Guilan university of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with a clinical diagnosis of Covid-19 including respiratory distress with a rate of more than 30 per minute and heart rate more than 125 beats per minute and shortness of breath and oxygen saturation less than 90%, despite receiving oxygen with a positive PCR test and Radiographs in CT SCANING or Chest X Ray, admitted to the intensive care unit. Uncontrollable fevers like T> 39 C. An laboratory evidence of increased inflammatory factors Patients 12 years and older Evidence of severe hemodynamic disturbance using moderate doses of norepinephrine or using a second dose of vasopressor Involvement of more than two vital organs (lungs, kidneys, liver, and heart)

Exclusion criteria

Exclusion criteria: Thrombocytopenia (Plt =20,000) Pregnancy Acute crisis due to sickle cell anemia Evidence of resin sensitivity

Design outcomes

Primary

MeasureTime frame
Improving the patient's clinical condition. Timepoint: Daily. Method of measurement: Evaluation of the presence of Respiratory distress, marked improvement in patients respiration rate, improvement in arterial blood gas condition and self-expression, improvement in patient's heart rate and improvement in patient's inflammatory tests 2-3 days after home perfusion. Inflammatory tests include D.DIMER, IL-6 LDH, FERRITIN, FIBRINOGEN, CRP.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Haghighi

Guilan University of Medical Sciences

mohaghighi@gums.ac.ir+98 13 3211 1319

Outcome results

None listed

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