MedTrace Logo

Acute Gastrointestinal Bleeding Peripheral Pulse Volume Changes

NCT06441201 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 13

Last updated 2025-12-11

No results posted yet for this study

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.

Conditions

  • GastroIntestinal Bleeding

Interventions

DIAGNOSTIC_TEST

Pulse flowmeter

Measures peripheral pulse volumes by an electrode applied non-invasively to the lower extremity (left or right) at the beginning of the endoscopic evaluation for the duration of the procedure, and up to 2 hours after the completion of the procedure.

Sponsors & Collaborators

Principal Investigators

  • Andrew Storm, MD · Mayo Clinic

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-06-13
Primary Completion
2025-09-22
Completion
2025-09-22

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06441201 on ClinicalTrials.gov