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Clinical Trials/IRCT201205305113N3
IRCT201205305113N3CompletedPhase 3

The effect of N-Acetyle Systeine in preventing contrast induced nephropathy in patients with different stages of chronic kidney diseases

ephrology Research Center, Tehran University of Medical Sciences0 sites549 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Phase 3
Status
Completed
Sponsor
Enrollment
549

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 years to 99 years (—)
Sex
All

Inclusion Criteria

  • age more than 18; serum creatinine more than 1.5 mg/ dl ; not having AKI; not receiving nephrotoxine since 1 week before entering the study; signing the consent.
  • Exclusion criteria: the patients who undergo surgery in less than 1 week of contrast exposure; the patients who are in need for a nephrotoxine in less than five days after contrast exposure; the patients who need repeated contrast administration in less than five days of first exposure

Exclusion Criteria

  • Not provided

Investigators

Sponsor
ephrology Research Center, Tehran University of Medical Sciences

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