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Evaluation of the effect of plasmapheresis in the treatment of Covid 19

Evaluation of the effect of therapeutic plasma exchange in patients with acute respiratory distress syndrome caused by Covid 19 disease

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200405046958N2
Enrollment
42
Registered
2021-04-14
Start date
2021-03-10
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

Covid 19 induced acute respiratory distress syndrome. Covid 19 virus identified

Interventions

Intervention 1: Intervention group: Patients who underwent plasmapheresis for 3 days in addition to routine treatment (Includes ventilation supportive care, serum therapy, treatment with heparin or en

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to No maximum

Inclusion criteria

Inclusion criteria: The patient must be definitive case of Covid-19 based on positive PCR test. The patient must have clinical and paraclinical criteria for acute respiratory distress syndrome (ARDS) The patient age must be over 15 years There must be the informed consent of the patient or his/her legal guardian

Exclusion criteria

Exclusion criteria: The patient has unstable hemodynamics The patient has a history of previous acute cardiac infarction in the last 3 months The patient has a history of allergies to blood products

Design outcomes

Primary

MeasureTime frame
Death. Timepoint: first 30 days of hospital admission. Method of measurement: examination of vital signs.

Secondary

MeasureTime frame
Disease severity. Timepoint: 1st, 3rd and 7th day after ICU admission. Method of measurement: Use of SAPS3 and SOFA scoring systems.;ICU ward stay. Timepoint: Day 30 and 60 from hospital admission. Method of measurement: Patient visit.;Mechanical ventilation duration. Timepoint: All days of ICU admission. Method of measurement: Daily visit.;Changes in CRP and Ferritin inflammatory markers. Timepoint: Days 0, 3 and 7 after ICU admission. Method of measurement: Serum levels of CRP and ferritin tests.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Moeini nodeh

Mashhad University of Medical Sciences

MoeiniNM@mums.ac.ir+98 51 3801 2742

Outcome results

None listed

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