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The effect of Mocozift® syrup on patients with COVID-19

The effect of natural medicine product (MOCOZIFT®) on clinical manifestations and para clinical features in patients with COVID-19: a randomized clinical trial

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT20221019056241N1
Enrollment
184
Registered
2022-10-24
Start date
2022-11-01
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

COVID-19 infection. Coronavirus infection, unspecified

Interventions

Intervention 1: Intervention group: patients in this group use 5 milliliters of natural product (brand name: Mocozift) produced in Behdane Baran pharmaceutical company, three times a day for five days

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age older than 18 years Confirmed COVID-19 infection using PCR test Prescription of Remdesivir for outpatient use Avoiding use of other traditional medicine or supplements during the trial signing the informed consent form

Exclusion criteria

Exclusion criteria: Participating in other clinical trials History of hypersensitivity reactions to natural or herbal medicines

Design outcomes

Primary

MeasureTime frame
The score of dyspnea severity according to Modified Medical Research Council Dyspnea Scale. Timepoint: One day before medicinal intervention and fifth day of intervention. Method of measurement: Modified Medical Research Council Dyspnea Scale.;Cough severity. Timepoint: One day before medicinal intervention and fifth day of intervention. Method of measurement: Cough visual analogue scale.;Appetite. Timepoint: One day before medicinal intervention and fifth day of intervention. Method of measurement: Simplified Nutritional Appetite Questionnaire (SNAQ).;Fatigue severity. Timepoint: One day before medicinal intervention and fifth day of intervention. Method of measurement: Fatigue Severity Scale (FSS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBabak Daneshfard

Shahid Beheshti University of Medical Sciences

babakdaneshfard@gmail.com+98 21 2712 3000

Outcome results

None listed

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