Skip to content

The Effect of Spironolactone on Acute Kidney Injury in Patients Undergoing Coronary Angiography

The Effect of Spironolactone on Acute Kidney Injury in Patients Undergoing Coronary Angiography

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03329443
Enrollment
490
Registered
2017-11-06
Start date
2017-09-01
Completion date
2018-09-04
Last updated
2018-09-10

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

Conditions

Acute Kidney Injury, Contrast-induced Nephropathy, IHD

Keywords

spironolactone

Brief summary

an interventional study to measure the possible effects of spironolactone ( an aldosterone antagonist) on the incidence of acute kidney injury after coronary angiography

Interventions

DRUGSpironolactone

each patient will receive 200 mg of spironolactone as per his/her angiography premedications

DRUGPlacebo Oral Tablet

Each patient will receive a placebo tablet as per his/her angiography premedications

Sponsors

Ministry of Health-Basra Health Directorate-Al-Sader Teaching Hospital
CollaboratorUNKNOWN
Alhasan Mujtaba Abdul-Wahid
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients admitted to angiography unit * over 18 * informed consent

Exclusion criteria

* acute renal failure before 7 days * spironolactone contraindications * hyperkalemia (S.K. \>5.5 mEq/L) * documented tumor * actively taking NSAIDs, Ciclosporin, Cisplatin,

Design outcomes

Primary

MeasureTime frameDescription
Acute kidney injury by K-DIGO guidelines48-72 hrsan absolute elevation of serum creatinine of 0.5mg/dl or 25% above baseline

Secondary

MeasureTime frameDescription
acute kidney injury by NGAL6 hoursassessment of serum NGAL at admission and after 6 hrs to detect possible AKI in selected patients

Other

MeasureTime frameDescription
safety outcome: serum potassium6 hrsserum potassium after 6 hrs of angio

Countries

Iraq

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026