Skip to content

The effect of interferon on the treatment of covid19 patients

Evaluation of interferon treatment in high-risk covid19 patients in Qom

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160118026097N3
Enrollment
60
Registered
2020-05-31
Start date
2020-03-20
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

COVID19.

Interventions

Sponsors

Ghoum University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Laboratory confirmation of Covid19 infection with reverse transcription polymerase chain reaction (RT-PCR) from any diagnostic sampling source A new organ dysfunction related to Covid19 Being an adult

Exclusion criteria

Exclusion criteria: Intention to commit suicide (interfering with interferon (IFN) -b1b). Sensitivity or sensitivity reaction to Lupinavir / Ritonavir or IFN-ß1b recombinant, including toxic epidermal necrolysis, Stevens-Johnson syndrome, erythema or angioedema syndrome. ALT above 5 times normal Use of drugs that are contraindicated with lopinavir / ritonavir and should not be substituted or discontinued during the study period, such as CYP3A inhibitors. pregnancy.Eligible female participants are tested at gestational age before enrolling in the study for pregnancy. HIV Vulnerable groups

Design outcomes

Primary

MeasureTime frame
Death within 30 days of hospitalization. Timepoint: every day. Method of measurement: View.

Secondary

MeasureTime frame
Days without organ support (for example, supplemental O2, mechanical ventilation, dialysis and vasopressors). Timepoint: Time interval: 28 days. Method of measurement: View.;Results of RT-PCR in lower respiratory samples. Timepoint: Time interval: At the time of entering the study and one week after treatment and repetition every week until the negative sample of the period. Method of measurement: test.;Body Failure Assessment Scores (SOFA). Timepoint: Time frame: days 1, 3, 5, 7, 14 and 28). Method of measurement: check list.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactjamsheed vafaeemanesh

Ghoum University of Medical Sciences

jvafaeemanesh@yahoo.com+98 25 3612 2526

Outcome results

None listed

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