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Clinical Trials/EUCTR2009-011175-70-GB
EUCTR2009-011175-70-GB
Active, not recruiting
Not Applicable

A randomised factorial trial of N-acetylcysteine prophylaxis and iso-osmolar versus low-osmolar contrast media on kidney function in patients at risk of contrast induced nephropathy following cardiac catheterisation for percutaneous coronary interventions - the CON NEC T” trial - CONNECT

iverpool Heart and Chest Hospital0 sitesApril 16, 2009
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DrugsFluimucilVISIPAQUEOptiray

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
iverpool Heart and Chest Hospital
Status
Active, not recruiting
Last Updated
13 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 16, 2009
End Date
TBD
Last Updated
13 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
iverpool Heart and Chest Hospital

Eligibility Criteria

Inclusion Criteria

  • •eGFR \< 60 ml/m (as calculated by modified MDRD equation with local laboratory correction factor)
  • •Are the trial subjects under 18? no
  • •Number of subjects for this age range:
  • •F.1\.2 Adults (18\-64 years) yes
  • •F.1\.2\.1 Number of subjects for this age range
  • •F.1\.3 Elderly (\>\=65 years) yes
  • •F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • •1\. Patients who had coronary angiography or other procedure with contrast exposure (CTPA etc.) within 2 weeks of PCI
  • •2\. Unable to consent
  • •3\. Patients undergoing angiographic investigations as a prelude to planned cardiac surgery
  • •4\. Cardiogenic shock
  • •5\. Unlikely to attend for follow up blood tests
  • •6\. Presence of non cardiac illness that might affect life expectancy
  • •7\. Any previous allergic reaction to contrast media or NAC

Outcomes

Primary Outcomes

Not specified

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