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NCT03238391

Ischemic Preconditioning for Prevention of Contrast Nephropathy in The Emergency Department

Status unknown NA Last updated 3 August 2017
What this trial tests

NA trial testing Ischemic preconditioning in Contrast-induced Nephropathy in 350 participants. Status unknown.

Timeline
15 August 2017
Primary endpoint
15 February 2018
15 February 2018

Quick facts

Lead sponsorDerince Training and Research Hospital
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposeprevention
Enrollment350
Start date15 August 2017
Primary completion15 February 2018
Estimated completion15 February 2018

Drugs / interventions tested

Conditions studied

Sponsor

Derince Training and Research Hospital

Who can join

18 and older, any sex, with Contrast-induced Nephropathy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to demonstrate the effectiveness of ischemic preconditioning in the emergency department to prevent contrast induced nephropathy

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Ischemic preconditioning

Trials testing the same drug.

Other recruiting trials for Contrast-induced Nephropathy

Currently open trials in the same condition.

Other Derince Training and Research Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03238391.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing