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Effect of Nicorandil on contrast media-induced acute kidney injury

A clinical trial of the comparison of the effect of oral Nicorandil plus hydration with hydration alone on serum creatinine in high-risk patients after receiving contrast

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016033118389N4
Enrollment
128
Registered
2016-04-25
Start date
2016-04-20
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

Acute renal failure. Drug- and heavy-metal-induced tubulo-interstitial and tubular conditions

Interventions

Intervention 1: Control group: All patients will be received intravenous hydration (2 liters normal saline From 2 h before to 6 h after contrast intake). Intervention 2: Intervention group: All patien
Causes sustained dilation of both the arterial resistance and conductive vessels. This drug is an anti-angina medication that has the dual properties of nitrate and K+ATP channel agonist.
Treatment - Drugs
Control group: All patients will be received intravenous hydration (2 liters normal saline From 2 h before to 6 h after contrast intake)
Intervention group: All patients will be received Nicorandil 20 mg ?tablet (two hours before contrast intake) plus intravenous hydration (2 liter Normal saline from 2 h before to 6 h after injection

Sponsors

Qom University of Medical Sciences and Health Services Vice chancellor
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 90 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria were the existence of at least one risk factor of contrast-induced nephropathy, including 1) Moderate systolic heart failure [30% 75 years 4) Moderate renal insufficiency (1/5mg/ dL 2 mg/dL and preexisting dialysis 6- Exposure to contrast medium 48 h pre- and post-coronary angiography 7- Receive of diuretics, N-acetylcystein, sodium bicarbonate, Theophylline, Dopamine, Fenoldopam and NSAID’S during the study 8- Needs to continuous hydration therapy (e.g., sepsis) 9-severe heart failure (EF<=30%)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Serum creatinine. Timepoint: Before and 48 h after contrast intake. Method of measurement: laboratory Kit (enzymatic method).

Countries

Iran (Islamic Republic of)

Contacts

Public Contactleili Iranirad

Qom University of Medical Sciences, Qom, Iran

liranirad@gmail.comlirani@muq.ac.ir+98 25 3612 2717

Outcome results

None listed

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