Clinical Trials Directory

Trials / Completed

CompletedNCT03867994

Comparison of Carvedilol and Atorvastatin for Preventing of Contrast-Induced Nephropathy.

Comparison of Carvedilol and Atorvastatin for Prevention of Contrast-Induced Nephropathy After Cardiac Catheterization

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
144 (actual)
Sponsor
rabab ahmed mohamed · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This prospective study is intended to evaluate if carvedilol has any potential protective effect over atorvastatin on the development of contrast-induced nephropathy (CIN) following cardiac catheterization in patients with moderate to high risk for CIN.

Detailed description

This study enrolled 150 patients planned for CC, and randomly assigned for one of the three groups. Group (A)include 49 patients who received two atorvastatin dose 80 mg 12 hours before CC and 40 mg just before CC. Group (B) include 48 patients who received 12.5 mg carvedilol twice daily for 7 days before CC and continue for 24hrs after the day of CC, Group (C) include 47 patients who only hydrated with saline. All included patients were hydrated with saline intravenous 0.9 sodium chloride (NaCl) at 0.5-1 mg/kg/hour for 4-6 hours before and 4-6 hours after cardiac catheterization. Serum creatinine(Scr), blood urea nitrogen (BUN) and estimated glomerular filtration rate were evaluated at the baseline and after 48 from CC. Serum neutrophil-associated lipocalin (NGAL) was evaluated after 4 hours from CC.

Conditions

Interventions

TypeNameDescription
DRUGAtorvastatin
DRUGCarvedilol
DRUGsaline

Timeline

Start date
2016-02-01
Primary completion
2017-05-15
Completion
2017-05-15
First posted
2019-03-08
Last updated
2019-03-12

Source: ClinicalTrials.gov record NCT03867994. Inclusion in this directory is not an endorsement.