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Preventive effect of curcumin in cardiac arrhythmia

Evaluation of curcumin effect on plaque rupturing serum biomarkers and atrial and ventricular arrhythmia in unstabl angina patients.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013102315122N1
Enrollment
40
Registered
2014-01-17
Start date
2013-11-05
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

I20. Preinfarction syndrome

Interventions

Intervention 1: Control: Tab Placebo four times per day for two weeks from admission day. Intervention 2: Intervention: Tab Curcumin 500 mg four times per day for two weeks from addmission date.
Treatment - Drugs
Control: Tab Placebo four times per day for two weeks from admission day
Intervention: Tab Curcumin 500 mg four times per day for two weeks from addmission date

Sponsors

Mashad University of Medical Sciences, Pharmaceutical Research Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age>18; diagnosis of unstable angina with clinic and para clinic finding. Exclusion criteria: Renal and hepatic failure; infectious diseases; NSIADS and immunosuppresion drugs consumption; curcumin sensitivity; pregnancy and feeding; malignancy; chronic inflammatory disease; cardiac arrhythmia; malabsorption syndromes

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Frequency of atrial and ventricular arrhythmia. Timepoint: Between first day to 30th day post unstable angina. Method of measurement: ECG-heart exam.

Secondary

MeasureTime frame
Changes in myeloperoxidase serum concentration. Timepoint: in day 0,5,10,15 post unstable angina. Method of measurement: laboratory.;Changes in matrix metaloproteinase serum concentration. Timepoint: in day 0,5,10,15 post unstable angina. Method of measurement: laboratory.;Changes in IL-18 serum concentration. Timepoint: in day 0,5,10,15 post unstable angina. Method of measurement: laboratory.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoumeh Salari

Mashad University Of Medical Sciences

salarim@mums.ac.ir+98 51 1842 3754

Outcome results

None listed

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