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The effects of Ginger in treatment COVID-19

The effects of Ginger on clinical manifestations and paraclinical features of patients with COVID-19: A randomized double-blind placebo-control clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200506047323N1
Enrollment
84
Registered
2020-05-23
Start date
2020-11-21
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 disease. COVID-19, virus not identified

Interventions

Intervention 1: Intervention group: The standard treatment regimen for COVID-19 along with a Ginger-based herbal medicine (Vomigone 500 mg tablets, registration number: 9406633051781240, Dineh Iran Ph

Sponsors

Bandare-abbas University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age =18 years Positive polymerase chain reaction (PCR) test for COVID-19 or/and lung involvement in imaging Primary clinical symptoms Hospitalized Signing informed consent and willingness of study participant to accept randomization to any assigned treatment arm

Exclusion criteria

Exclusion criteria: Underlying diseases, including chronic hepatitis, cirrhosis, cholestatic liver diseases, cholecystitis, and peptic ulcers Use of anticoagulant drugs like warfarin, and hormonal drugs History of allergy to ginger Pregnancy and breastfeeding

Design outcomes

Primary

MeasureTime frame
SARS-CoV-2 clearance. Timepoint: Before intervention and day 7. Method of measurement: PCR test.;Fever. Timepoint: Before intervention and daily during the study. Method of measurement: Thermometer.;White blood cell count. Timepoint: Before intervention and day 7. Method of measurement: Labratory.

Secondary

MeasureTime frame
Hospital admission. Timepoint: During the intervention. Method of measurement: Questionnaire.;Incidence of serious adverse events. Timepoint: Before intervention and daily during the study. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Fathalipour

Bandare-abbas University of Medical Sciences

m.fathalipour@hums.ac.ir+98 76 3371 0406

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 25, 2026