CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 266 enrolled
Drug / intervention
Remote ischemic postconditioning +1 moreprocedure
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01113008
NCT01113008N/ACompleted
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Remote Ischemic Postconditioning. Can it Prevent Myocardial Injury During Percutaneous Coronary Intervention?

Hospital Universitario Virgen de la Victoria·interventional·Posted Apr 29, 2010·Updated Jan 21, 2015

In Brief

A clinical study evaluating Remote ischemic postconditioning and Control group for Myocardial Reperfusion Injury. Completed, enrolled 266 participants across 1 site.

Detailed Summary

The aim of this study is to evaluate the phenomenon of remote ischemic post-conditioning in humans. The minor myocardial damage associated with percutaneous revascularization procedures may be attenuated by producing controlled ischemia in the arms immediately after carrying out these procedures (remote ischemic post-conditioning). The justification and design of this clinical trial has been reported: Cardiology. 2011;119(3):164-9.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyocardial Reperfusion Injury
CountriesSpain
CollaboratorsFUNDACIÓN IMABIS, Red Temática de Investigación Cooperativa en Enfermedades Cardiovasculares

Timeline

N/ACompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedApr 29, 2010
Enrollment StartFeb 1, 2009
Primary CompletionFeb 1, 2012
Study CompletionMay 1, 2012
TodayJul 2, 2026
Enrollment to primary: 3 yearsPosted 16.2 years ago

Interventions

Remote ischemic postconditioningprocedure

Patients assigned to remote ischemic postconditioning will undergo three 5-minute cycles of ischemia using a blood-pressure cuff at 200 mmHg, placed on the non-dominant arm, interrupted twice for 5 minutes with the cuff deflated

Control groupprocedure

In the control group the procedure will be limited to placing a deflated blood-pressure cuff (pressure: 0 mmHg) for 25 minutes.