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NCT01878344Active, not recruitingPhase 3

Effects of N-acetyl Cysteine During Primary Percutaneous Coronary Intervention

Effects of N-acetyl Cysteine on Major Cardiac and Cerebral Events in Patients Undergoing Primary Percutaneous Coronary Intervention Who Have Moderate to High Risk For Contrast Induced Nephropathy

Source: ClinicalTrials.gov · Last updated 20 May 2025

Brief summary (registry, in English)

The aim of this study is to evaluate the effects of N-acetyl cysteine on major cardiac and cerebral events in patients undergoing primary percutaneous coronary intervention who have moderate to high risk for contrast induced nephropathy. In a sub-group of patients coronary flow reserve will be evaluated.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
100 (actual)
First submitted
12 Jun 2013
Start date
Jan 2013
Primary completion date
Jan 2018
Lead sponsor
Suleyman Demirel University
NCT number
NCT01878344

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 100
  • From Jan 2013 to the primary completion date, Jan 2018
  • 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

  • Use of corticosteroids
  • Blood pressure of \>180/100mmHg despite anti-hypertensive therapy

Other illness

  • Infection
  • Renal failure requiring dialysis
  • Hepatic failure
  • Allergy to NAC
  • History of Asthma
  • Malignancy

Age

  • Patients \>18 years old with moderate to high risk for contrast induced nephropathy undergoing percutaneous coronary intervention

Other

  • Low risk for contrast induced nephropathy (Mehran Score \<5)
  • Use of nephrotoxic agents (NSAIDs, aminoglycosides,recent contrast injection...)
  • Pregnancy, Lactation
  • Chronic nitrate usage
  • Leucocytosis,Thrombocytosis,Anemia

Who the study is looking for

  • Patients with Acute ST Elevation Myocardial Infarction undergoing Primary Percutaneous Coronary intervention Who Have Moderate to High Risk For Contrast Induced Nephropathy (Mehran Score ≥5)

Age in the registry: 18 years to 85 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Suleyman Demirel University
Coordinator of this site? Confirm its status
IspartaTurkey (Türkiye)Unknown status

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