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

NCT03329443 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 490

Last updated 2018-09-10

No results posted yet for this study

Summary

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

Conditions

Interventions

DRUG

Spironolactone

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

DRUG

Placebo Oral Tablet

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

Sponsors & Collaborators

  • Ministry of Health-Basra Health Directorate-Al-Sader Teaching Hospital

    collaborator UNKNOWN
  • Alhasan Mujtaba Abdul-Wahid

    lead OTHER

Principal Investigators

  • Alhasan Mujtaba, BCPS · Baghdad University/College of Pharmacy/Department of Clinical Pharmacy

  • Mohammed A Taher, Ph.D. · Baghdad University/College of Pharmacy/Department of Biochemistry

  • Mazin A Hazzaa', Ph.D. · Al-Sader teaching Hospital/Basra Cardiac Center/M.D. Cardiologist

  • Hassan M Al Rubaye, Ph.D · Al-Sader teaching Hospital/Basra Cardiac Center/M.D. Cardiologist

  • Assad H Kata, Ph.D · Al-Sader teaching Hospital/Basra Cardiac Center/M.D. Cardiologist

  • Hayder K Abdullkreem, M.Sc · Head of the clinical laboratory department/ Al-Sader teaching hopital

  • Hamid A Abdulsada, Ph.D · Al-Sader teaching Hospital/Basra Cardiac Center/M.D. Cardiologist

  • Abdul Ameer A Abdul Hameed, PH.D · Al-Sader teaching Hospital/Basra Cardiac Center/M.D. Cardiologist

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-09-01
Primary Completion
2018-09-01
Completion
2018-09-04

Countries

  • Iraq

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03329443 on ClinicalTrials.gov