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Efficacy and safety of tofacitinib on clinical improvement in patients with COVID19

Efficacy and safety of tofacitinib on clinical improvement in hospitalized patients with COVID19: A randomized, double blind multi-centre clinical trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190804044429N7
Enrollment
240
Registered
2021-10-27
Start date
2021-10-22
Completion date
Unknown
Last updated
2021-11-01

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

Conditions

COVID-19 pneumonia. Covid-19 disease

Interventions

Intervention 1: Intervention group: all the patients received remdesivir (200 mg on the first day followed by 100 mg daily for five days and, corticosteroid therapy ( Dexamethasone 8 mg or equivalent

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Hospitalization with oxygen saturation less than 94% COVID-19 diagnosis according to chest CT scan or RT-PCR

Exclusion criteria

Exclusion criteria: Pregnancy lactating women Severe liver failure (Child-pugh C) or liver enzymes more than 3 times normal Renal failure (glomerular filtration less than 30 ml / min) Chronic use of immunosuppressive drugs or corticosteroids Absolute lymphocyte count less than 500 per cubic millimeter Absolute neutrophil counts less than 1000 per cubic millimeter

Design outcomes

Primary

MeasureTime frame
Improving the clinical symptoms of patients with covid-19. Timepoint: Day one, day seven, day 14, day 28. Method of measurement: eight-category ordinal scale.

Secondary

MeasureTime frame
Mortality rate. Timepoint: During hospitalization and on days 14 and 28. Method of measurement: Observation.;Admission in intensive care units. Timepoint: During hospitalization. Method of measurement: Observation.;Ventilator need. Timepoint: During hospitalization. Method of measurement: Observation.;Incidence of possible side effects. Timepoint: During hospitalization. Method of measurement: Observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMonireh Ghazaeian

Mazandaran University of Medical Sciences

ghazaeianm@gmail.com+98 11 3334 3011

Outcome results

None listed

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