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Resveratrol in COVID19

Evaluation of the effect of Resveratrol on the effectiveness of antiviral drug regimen in patients with COVID-19

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200112046089N1
Enrollment
50
Registered
2020-06-25
Start date
2020-06-14
Completion date
Unknown
Last updated
2020-07-13

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

Conditions

COVID19. COVID-19, virus identified

Interventions

Intervention 1: Intervention group: 1 Tab resveratrol (500mg) from Sumabe, daily until 14 days in addition to routine drugs. Intervention 2: Control group: this group doesn't receive extra drugs and

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Polymerase chain reaction (PCR) confirmed infection with SARS CoV2 Lung involvement confirmed with chest imaging Hospitalized with: Fever (axillar or oral temperature = 38.0 °centigrade(C) or =38.6°centigrade tympanic or rectal) or Respiratory rate >24/min Or Cough Less than 8 days since illness onset Willingness of study participant to accept random assignment to any treatment arm Acceptance of non-participation in another study before the 28th day of the study

Exclusion criteria

Exclusion criteria: Autoimmune diseases (lupus, MS, etc.) Hepatic failure Hepatit B and C pregnant and lactating women

Design outcomes

Primary

MeasureTime frame
Recovery time. Timepoint: Duration of treatment. Method of measurement: Evaluation of clinical symptoms.;Repiratory signs. Timepoint: daily. Method of measurement: clinical evaluation and questionnaire.;Pulmonary Condition. Timepoint: Before intervention and 14 days after intervention. Method of measurement: CT scan.

Secondary

MeasureTime frame
Blood oxygen saturation percentage. Timepoint: Before and 14 days after starting treatment. Method of measurement: Pulse oximeter.;C-Reactive Protein (CRP). Timepoint: Before and fourteen days after starting treatment. Method of measurement: ?ELISA (enzyme-linked immunosorbent assay).;IL6. Timepoint: Before and 14 days after starting treatment. Method of measurement: ELISA (enzyme-linked immunosorbent assay).;IL1. Timepoint: Before and 14 days after starting treatment. Method of measurement: ELISA (enzyme-linked immunosorbent assay).;CBC. Timepoint: Before and 14 days after starting treatment. Method of measurement: Cell Counter.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactArash Alghasi

Ahvaz University of Medical Sciences

alghasi-a@ajums.ac.ir+98 61 3374 3289

Outcome results

None listed

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