Atorvastatin Effect on Contrast Induced Nephropathy in Diabetic Patients Undergoing Elective Coronary Intervention

Sponsor
Mohamed Abdelfatah (Other)
Overall Status
Completed
CT.gov ID
NCT04375787
Collaborator
(none)
200
1
2
2.6
77.1

Study Details

Study Description

Brief Summary

Investigate of the potential benefit of acute pretreatment with high dose atorvastatin (80 mg) in reduction of the incidence of CIN in diabetic patients indicated for elective coronary intervention.

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

The study is a prospective, multi-center, randomized, placebo-controlled study. The ethical committee of the Faculty of Medicine, Assiut University approved the study protocol.

200 diabetic patients with indication for coronary intervention participated in the study. 100 patients were randomly assigned to receive atorvastatin (80 mg) just before coronary intervention (statin group) and 100 patients received placebo (control group). An informed written consent for participating in the study was obtained from each participant.

Exclusion criteria:
  1. Current statin treatment within the previous three months.

  2. Chronic renal failure patients on renal dialysis, or serum creatinine more than 1.5 mg/dl.

  3. Severe co-morbidities i.e. patients with cancer, advanced liver cirrhosis.

  4. Contraindications to statin therapy.

  5. Contrast media injection within the preceding 10 days.

  6. Pregnancy.

  7. Refusal of consent. (B) Methodology:

All study patients were subjected to:
  1. Full clinical history: including age, sex, history of smoking, hypertension, history of previous percutaneous coronary intervention (PCI), duration of diabetes mellitus (DM) and type of anti-DM treatment.

  2. Thorough physical examination focusing on:

  • General examination including intra-procedural hemodynamic assessment.

  • Cardiac examination to elicit manifestations of heart failure.

  1. Echocardiography searching for wall motion abnormalities and estimation of left ventricular systolic function.

  2. Initial venous blood samples for determination of hemoglobin level and serum creatinine before the procedure. Follow up for serum creatinine at 48 hours post-procedure was done.

CIN was stated as a raising of serum creatinine of more than 25% or ≥0.5 mg/dl (44 μmol/l) from initial level within 48 hours of the angiographic procedure and after excluding other factors that may cause nephropathy such as nephrotoxic drugs.

  1. All patients received clopidogrel (600 mg) or ticagrelor (180 mg). Any nephrotoxic drugs (i.e., metformin, non-steroidal anti-inflammatory drugs) were withdrawn on admission.

  2. Coronary intervention was done using the same non-ionic, low-osmolar contrast medium (Iopamidol; Scanlux, Sanochemia, Austria) in all cases.

After the procedure, TIMI flow of the culprit artery was assessed, as well as the volume of used contrast media and time of X-ray exposure.

  1. Statistical analysis:

Data were processed by statistical package for the social sciences (SPSS, version 20. 0). Descriptive statistics for interval and ordinal variables were calculated such as the ranges, means, and standard deviations, whereas, for categorical variables, the frequencies and percentages were reported. Student t-test or paired t-test, as appropriate, were used to compare normal and continuous variables. Chi-square test was used for comparing categorical variables. The level of significance was stated at P < 0.05. Receiver operating curves (ROC) were plotted and area under the curve (AUC) was assessed for some studied variables. Sensitivity and specificity were calculated at a cutoff point. A p value of <0.05 was considered significant.

Study Design

Study Type:
Interventional
Actual Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
200 diabetic patients with indication for coronary intervention participated in the study. 100 patients were randomly assigned to receive atorvastatin (80 mg) just before coronary intervention (statin group) and 100 patients received placebo (control group).200 diabetic patients with indication for coronary intervention participated in the study. 100 patients were randomly assigned to receive atorvastatin (80 mg) just before coronary intervention (statin group) and 100 patients received placebo (control group).
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
High Dose Atorvastatin Raises Threshold of Contrast Induced Nephropathy in Diabetic Patients Undergoing Elective Coronary Intervention
Actual Study Start Date :
Mar 15, 2020
Actual Primary Completion Date :
Jun 2, 2020
Actual Study Completion Date :
Jun 2, 2020

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Statin group

100 patients were randomly assigned to receive atorvastatin (80 mg) just before coronary intervention

Drug: Atorvastatin
Patients received 80 mg atorvastatin before elective coronary angiography
Other Names:
  • statin
  • Placebo Comparator: Placebo group

    100 patients received placebo

    Drug: Atorvastatin
    Patients received 80 mg atorvastatin before elective coronary angiography
    Other Names:
  • statin
  • Outcome Measures

    Primary Outcome Measures

    1. Contrast Induced Nephropathy (CIN) [48 hours]

      CIN was defined as a rise of serum creatinine of more than 25% or ≥0.5 mg/dl (44 μmol/l) from baseline within 48 hours of the angiography

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    30 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • 200 diabetic patients with indication for coronary intervention participated in the study
    Exclusion Criteria:
    1. Current statin treatment within the previous three months.

    2. Chronic renal failure patients on renal dialysis, or serum creatinine more than 1.5 mg/dl.

    3. Severe co-morbidities i.e. patients with cancer, advanced liver cirrhosis.

    4. Contraindications to statin therapy.

    5. Contrast media injection within the preceding 10 days.

    6. Pregnancy.

    7. Refusal of consent.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Assiut University Assiut Egypt 71515

    Sponsors and Collaborators

    • Mohamed Abdelfatah

    Investigators

    • Study Chair: Ayman Ibrahem, MD, Assiut University
    • Study Director: Ahmed Abdel-Galeel, MD, Assiut University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Mohamed Abdelfatah, investigator, Assiut University
    ClinicalTrials.gov Identifier:
    NCT04375787
    Other Study ID Numbers:
    • Atorvastatin in elective CA
    First Posted:
    May 5, 2020
    Last Update Posted:
    Feb 16, 2022
    Last Verified:
    Feb 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 16, 2022