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Effects of nano curcumin supplementation on the reduction of inflammation and mortality in patients with coronavirus 2019 admitted to ICU ward of imam Reza hospital in Tabriz

Effects of nano curcumin supplementation on the reduction of inflammation and mortality in patients with coronavirus 2019 admitted to ICU ward of Imam Reza hospital in Tabriz

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200324046851N1
Enrollment
86
Registered
2020-04-03
Start date
2020-03-29
Completion date
Unknown
Last updated
2020-04-21

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

Conditions

COVID-2019. COVID-19, virus identified

Interventions

Intervention 1: Intervention group: Nanocurcumin, which is curcumin, is derived from the yellow-cucumber plant, which is embedded in nano-lipid structures for further absorption. The drug is manufactu

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Confirmation of positive for coronavirus by RT-pcr Willingness to cooperate In accordance with clinical diagnosis or etiologic criteria for coronavirus pneumonia (COVID-19). Able to sign informed consent

Exclusion criteria

Exclusion criteria: Nutrition and antioxidant supplements and alpha lipoic acid during one month before study Pregnancy and lactation Severe immune suppression (HIV infection, long-term use of immunosuppressive agents) Unwillingness to continue cooperation

Design outcomes

Primary

MeasureTime frame
Expression of peripheral blood mononuclear cell (PBMC)- Genes Expressed in Nano-Curcumin Patients with Control Group (Before and After Treatment). Timepoint: At baseline and 14 days later. Method of measurement: Real time Polymerase chain reaction.;The secretion rate of peripheral blood mononuclear cell (PBMC)-treated cytokines in nano-curcumin patients and control group (before and after treatment). Timepoint: At baseline and 14 days later. Method of measurement: Elisa kit.;Clinical features. Timepoint: At baseline and 14 days later. Method of measurement: Clinical observations by specialists.;Laboratory observations. Timepoint: At baseline and 14 days later. Method of measurement: Review by a pulmonary specialist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMajid Ahmadi

Tabriz University of Medical Sciences

Ahmadi.m@tbzmed.ac.ir+98 41 3336 4665

Outcome results

None listed

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