Clinical Trials Directory

Trials / Completed

CompletedNCT06871358

The Effect of Atorvastatin 80 mg on Hs-CRP/Albumin Ratio in Reducing Thrombus Burden in PCI-STEMI Patients

The Effect of Pre- and Post-Administration of 80 mg Atorvastatin on Hs-CRP/Albumin Ratio in Reducing Thrombus Burden in STEMI Patients Undergoing Primary PCI

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Universitas Sebelas Maret · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

40 STEMI patients who underwent primary PCI were subsequently allocated into two groups via a double-blind randomization method: An Atorvastatin 80 mg group and the control group. Levels of hs-CRP and albumin were assessed for both groups upon presentation at the emergency department before to initial PCI and were re-evaluated 24 hours after primary PCI. Thrombus burden was assessed using angiography with the TIMI Thrombus grade.

Detailed description

This study encompasses 40 STEMI patients who underwent primary PCI at Dr. Moewardi General Hospital in Central Java, Indonesia, between September and October. This study employed an experimental design with a pre-and-post technique, with participants recruited through sequential sampling. Patients were subsequently allocated into two groups via a double-blind randomization method. A treatment group was administered a loading dose of high-intensity statin (80 mg atorvastatin) upon initial presentation at the emergency department (ED), whereas the control group received no such intervention. Both cohorts received therapy in accordance with established guidelines prior to performing primary PCI. Levels of hs-CRP and albumin were assessed for both groups upon presentation at the emergency department before to initial PCI. In the treatment group, a second 80 mg dose of atorvastatin was provided 24 hours after the original dose. Both hs-CRP and albumin levels were re-evaluated 24 hours after primary PCI in both the control and treatment cohorts. Thrombus burden was assessed using angiography with the TIMI Thrombus grade

Conditions

Interventions

TypeNameDescription
DRUGAtorvastatin 80mg80 mg of Atorvastatin are loading in first medical contact (Emergency Department) before primary PCI
DRUGPlaceboOnly given a loading DAPT without loading Atorvastatin 80 mg

Timeline

Start date
2024-09-01
Primary completion
2024-10-30
Completion
2024-11-20
First posted
2025-03-11
Last updated
2025-03-11

Locations

1 site across 1 country: Indonesia

Source: ClinicalTrials.gov record NCT06871358. Inclusion in this directory is not an endorsement.