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Approval for the study was granted by the Lleida Health Region's Drug Research Ethics Committee. The assessment process involved 216 patients in total. A consistent distribution of sociodemographic and clinical factors was observed in both groups of the trial. A statistically significant decrease in peri-catheter bleeding and/or oozing was observed in the intervention group over the seven-day study period, indicated by an odds ratio of 0.6 and a 95
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