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Clinical trial of trans sodium crocetinate against COVID-19

Evaluation of the effect of trans sodium crocetinate in respiratory distress caused by COVID-19

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20081019001369N6
Enrollment
30
Registered
2020-05-17
Start date
2020-06-21
Completion date
Unknown
Last updated
2020-06-15

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

Conditions

Covid-19. COVID-19 Disease

Interventions

Intervention 1: Intervention group: In addition to the standard treatment regimen for COVID-19, the trans sodium crocetinate 1 mg/kg/day will be given i.v. for 1 weeks. Intervention 2: Control group:

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients with clinical diagnosis for Covid-19 disease, Patients with acute respiratory distress syndrome (ARDS), Patients not having kidney, liver and heart dysfunction according to clinical and laboratory findings PF ratio (the ratio of arterial oxygen partial pressure to fractional inspired oxygen) <300 ,

Exclusion criteria

Exclusion criteria: Allergic reactions to saffron Pregnancy or breast-feeding Multi organ dysfunction disease

Design outcomes

Primary

MeasureTime frame
Patients' mortality rate. Timepoint: During 7 days hospitalization. Method of measurement: Meedical Reports.

Secondary

MeasureTime frame
Days under ventilation. Timepoint: During 7 days hospitalization. Method of measurement: Meedical Reports.;Hospitalization days in ICU. Timepoint: During 7 days hospitalization. Method of measurement: Medical Report.;Getting multi organ dysfunction. Timepoint: During 7 days hospitalization. Method of measurement: Clinical and laboratory evaluation.;Improving PF ration. Timepoint: daily during 7 days hospitalization. Method of measurement: ratio calculated from PaO2/FiO2.;Improving Sofa (The sequential organ failure assessment ) score. Timepoint: the first day and during 7 days hospitalization. Method of measurement: According to clinical and laboratory evaluation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmirhoushang Mohammadpour

Mashhad University of Medical Sciences

MohamadpoorAH@mums.ac.ir+98 51 3180 1592

Outcome results

None listed

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