Acute Gastrointestinal Bleeding Peripheral Pulse Volume Changes

Status Enrolling by invitation

Clinical Trial Summary

The purpose and aim of this study are to compare changes in pulse volume to non-invasively predict active bleeding or high-risk stigmata in patients undergoing a gastrointestinal endoscopy to assess feasibility of the flow meter clinically.

Clinical Trial Description

The maximum change in volume of a limb segment during the cardiac cycle - pulse volume - will be monitored non-invasively along with standard vitals in patients with a suspected gastrointestinal bleed undergoing endoscopy. Pulse volume and vitals will be collected prior to and following endoscopy up to the point of dismissal from the endoscopy unit so that the data may be correlated with the endoscopic and clinical findings. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06441201
Study type	Observational
Source	Mayo Clinic
Contact
Status	Enrolling by invitation
Phase
Start date	June 13, 2024
Completion date	August 2024

View Details

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