Full Text View
Tabular View
No Study Results Posted
Related Studies
Acetylcysteine, Theophylline, and a Combination of Both in the Prophylaxis of Contrast-Induced Nephropathy (ATHENS)
This study has been completed.
First Received: June 26, 2007   No Changes Posted
Sponsor: Technische Universität München
Information provided by: Technische Universität München
ClinicalTrials.gov Identifier: NCT00492518
  Purpose

Several studies demonstrated a significant reduction of contrast-induced nephropathy (CIN; definition: increase in serum creatinine of >=0.5mg/dl and/or >=25% increase within 48h after contrast-medium) by acetylcysteine (A) or theophylline (T). However, the results are contradictory. Therefore, it was the aim of our double-blind study to compare the effects of A, T, a combination of A and T (A+T), and placebo (P).


Condition Intervention Phase
Contrast Induced Nephropathy
Kidney Diseases
Renal Failure
Adverse Effects
Drug: Acetylcysteine
Drug: Theophylline
Drug: Placebo
Phase IV

Study Type: Interventional
Study Design: Prevention, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study
Official Title: Acetylcysteine, Theophylline, and a Combination of Both in the Prophylaxis of Contrast-Induced Nephropathy: A Placebo Controlled Randomized Study

Resource links provided by NLM:


Further study details as provided by Technische Universität München:

Primary Outcome Measures:
  • The incidence of contrast induced nephropathy, defined as an increase of serum creatinine of at least 0.5 mg/d and/or 25% within 48 hours of contrast-medium application (comparison of treatment groups to placebo) [ Time Frame: 48h after the application of contrast-medium ]

Secondary Outcome Measures:
  • Change in serum creatinine 48h after contrast medium compared to pre-contrast serum creatinine. Multiple regression analysis of risk-factors of CIN with “Y=Maximum increase of serum creatinine compared to baseline within 48h” [ Time Frame: 48h ]

Enrollment: 254
Study Start Date: February 2002
Study Completion Date: October 2004
Detailed Description:

Contrast-induced nephropathy (CIN) is the third leading cause of hospital-acquired acute renal failure (ARF). Accounting for 12% of ARF cases, CIN is defined as an increase of serum creatinine of at least 0.5 mg/d (“Barrett´s definition”) and/or 25% within 48 hours of contrast-medium application. CIN is associated with prolonged hospitalisation and increased mortality. CIN frequency depends on several risk-factors including pre-existing renal dysfunction, high amounts of contrast-medium, diabetes, and concurrent use of nephrotoxic drugs. CIN incidence is low in the absence of risk-factors; however, in high-risk patients, CIN occurs in more than 50% of patients.

A variety of prophylactic approaches have been investigated. Despite nephro-protective effects of hydration with saline or with sodium bicarbonate, other trials reported CIN-incidences between 20 and 50% despite hydration. Several studies and two recent meta-analyses demonstrated a significant reduction of renal impairment after contrast-medium using medical prophylaxis with the adenosine antagonist theophylline. However, a recent trial failed to prove prophylactic effects of theophylline.

The antioxidant acetylcysteine (ACC) was effective in patients with impaired renal function in at least six studies, but it was not preventive in at least 21 trials and two recent meta-analyses. A recent study comparing the prophylactic efficacy of theophylline and acetylcysteine demonstrated superior prophylactic effects of theophylline. Nevertheless, this study did not include a placebo group, was not restricted to patients with impaired renal function and exclusively enrolled ICU-patients.

Therefore, we performed a double-blinded study to compare the effects of acetylcysteine, theophylline, a combination of both, and placebo in patients with impaired renal function (serum creatinine >=1.3mg/dl) parenterally receiving >=100ml of contrast-medium.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Impaired renal function (serum creatinine >=1.3mg/dl)
  • >=100ml of contrast-medium
  • Age >= 18years
  • Informed consent

Exclusion Criteria:

  • Previous dialysis and/or haemofiltration
  • Pre-treatment with acetylcysteine and/or theophylline within the last 2 days,
  • Pregnancy
  • Contraindications to theophylline (untreated high grade arrhythmia or a history of seizures) or acetylcysteine (known allergy).
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00492518

Locations
Germany
Klinikum Rechts der Isar; Technical University of Munich
Munich, Germany, D-81675
Sponsors and Collaborators
Technische Universität München
Investigators
Principal Investigator: Wolfgang Huber, MD Technische Universität München
  More Information

No publications provided

Study ID Numbers: ACC-Theo-1.3
Study First Received: June 26, 2007
Last Updated: June 26, 2007
ClinicalTrials.gov Identifier: NCT00492518     History of Changes
Health Authority: Germany: Ethics Commission

Keywords provided by Technische Universität München:
Contrast Induced Nephropathy
Prophylaxis
Theophylline
Acetylcysteine
Coronary angiography

Additional relevant MeSH terms:
Respiratory System Agents
Anti-Infective Agents
Vasodilator Agents
Renal Insufficiency
Antioxidants
Molecular Mechanisms of Pharmacological Action
Physiological Effects of Drugs
Urologic Diseases
Therapeutic Uses
Free Radical Scavengers
Acetylcysteine
Kidney Diseases
Antidotes
Anti-Asthmatic Agents
Enzyme Inhibitors
Cardiovascular Agents
Antiviral Agents
Protective Agents
Pharmacologic Actions
Phosphodiesterase Inhibitors
Autonomic Agents
Expectorants
Peripheral Nervous System Agents
Bronchodilator Agents
N-monoacetylcystine
Theophylline
Kidney Failure

ClinicalTrials.gov processed this record on November 30, 2009