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Evaluation of curcumin in pre-procedural cardiac injury following angioplasty in patients with ischemic heart diseases

Randomized trial of curcumin in pre-procedural cardiac injury following angioplasty in patients with ischemic heart diseases

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201603038307N13
Enrollment
100
Registered
2017-04-28
Start date
2017-02-15
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

Effect of curcumin in pre-procedural cardiac injury following angioplasty in ischemic heart diseases patients. Ischemic heart diseases

Interventions

Intervention 1: Intervention: In curcumin group, all patients will be received totally 320mg oral curcumin before PCI plus the standard treatment. Intervention 2: Control: In the control group, patien
Treatment - Drugs
Intervention: In curcumin group, all patients will be received totally 320mg oral curcumin before PCI plus the standard treatment.

Sponsors

Vice chancellor for research, Tabriz University of Medical Sciences.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Ischemic heart diseases patients; age 18-80; undergoing of angioplasty with stent insertion; filling of consent form. Exclusion Criteria: Elevation of CK-MB and cTnI before PCI; history of CABG during last three months; history of previous MI; renal dysfunction (creatinine above 2.5 mg/dl); unsuccessful PCI; acute MI; cardiogenic shock; dialysis; pregnancy; inability in filling and understanding of the consent form; unconsented patients; patients who want to discontinue the study at any time

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
CK-MB level. Timepoint: Before, 8 and 24 hours after angioplasty. Method of measurement: ELISA kits.

Secondary

MeasureTime frame
CTnI level. Timepoint: Before, 8 and 24 hours after angioplasty. Method of measurement: ELISA kits.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Taher Entezari-Maleki

Tabriz University of Medical Sciences

tentezari@gmail.com+98 41 3339 2593

Outcome results

None listed

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