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NCT06871358Completed

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

Source: ClinicalTrials.gov · Last updated 11 Mar 2025

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
40 (actual)
First submitted
3 Mar 2025
Start date
1 Sept 2024
Primary completion date
30 Oct 2024
Lead sponsor
Universitas Sebelas Maret
NCT number
NCT06871358

What you commit to

  • Study type: Interventional
  • Participants enrolled: 40
  • From 1 Sept 2024 to the primary completion date, 30 Oct 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior statin therapy within the preceding 24 hours

Lab values

  • Hypersensitivity to statins, pregnancy, lactation, severe inflammatory conditions including active liver dysfunction, chronic kidney disease (eGFR \<30 mL/min), autoimmune disorders, malignancy, severe malnutrition, and

Other

  • STEMI beyond 24 hours from the onset of chest pain
  • Contraindications to statin administration.

Who the study is looking for

  • STEMI with onset less than 24 hour and undergo a Primary PCI

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
RSUD Dr Moewardi
Coordinator of this site? Confirm its status
SurakartaIndonesiaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.