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Evaluation of therapeutic effects of ZAX.1400.C05 on patients with coronavirus

Evaluation of therapeutic effects of ZAX.1400.C05 on symptomatic treatment and clinical features of patients with coronavirus: a randomized controlled clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210218050404N4
Enrollment
300
Registered
2022-02-24
Start date
2022-04-03
Completion date
Unknown
Last updated
2022-03-08

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

Conditions

COVID-19 viral disease. Coronavirus infection, unspecified

Interventions

Intervention 1: Intervention group: Dried powder of ZAX.1400.C05, made in the laboratory of medicinal plants of Fasa University of Medical Sciences, based on plant flavonoids, in the form of capsules,

Sponsors

Fasa University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Definitive diagnosis of COVID-19 disease by laboratory diagnostic kit from patient sputum Patient hemoglobin saturation (SPO2) between 85% and 93% in patients Detection of lung involvement by CT scan in patients The number of breaths per minute is between 25 and 30 in patients

Exclusion criteria

Exclusion criteria: History of allergies to herbal products Pregnancy and lactation Existence of liver and kidney diseases Inability of the patient to receive oral medication

Design outcomes

Primary

MeasureTime frame
Clinical signs. Timepoint: daily. Method of measurement: Evaluation form (questionnaire).;(VAS) Visual Analogue Scale. Timepoint: daily. Method of measurement: check list.;ESR (Erythrocyte sedimentation rate). Timepoint: Zero and fourteen days after the start of the intervention. Method of measurement: Standard sedimentation rate method.;C-Reactive Protein – CRP. Timepoint: Zero and fourteen days after the start of the intervention. Method of measurement: Autoanalyzer.;Liver enzymes SGOT, ALT, SGPT. Timepoint: Zero and fourteen days after the start of the intervention. Method of measurement: Autoanalyzer.;Renal indicators BUN, Creatinine. Timepoint: Zero and fourteen days after the start of the intervention. Method of measurement: Autoanalyzer.

Secondary

MeasureTime frame
Duration of hospitalization. Timepoint: daily. Method of measurement: check list.;Mortality. Timepoint: daily. Method of measurement: check list.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmin Dakhili Ardestani

Fasa University of Medical Sciences

amindakhiliardestani@yahoo.com+98 71 5335 9507

Outcome results

None listed

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