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Clinical Trial Summary

The investigators are conducting a randomized clinical trial, having as a primary objective, to compare vascular access time between distal and proximal radial approach. Secondary objectives include comparing incidence of distal and proximal radial artery occlusion, at 24 hrs and 30 days. As a tertiary objective investigators will compare the preference of the patients for each access in subsecuent interventional procedures.


Clinical Trial Description

Randomised Clinical Trial Permutted block asignation 1:1 Statistical Power 80% and Significance 5%. Sample Loss estimation - 15% Chi-square to categorical and T Student to numerical variables. Logistic regression binomial for adverse outcomes. If needed, an intention to treat analysis will be performed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05066074
Study type Interventional
Source Instituto Mexicano del Seguro Social
Contact
Status Enrolling by invitation
Phase N/A
Start date August 16, 2021
Completion date June 1, 2022

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