CompletedNot Applicable

Acute Gastrointestinal Bleeding Peripheral Pulse Volume Changes

United States13 participantsStarted 2024-06-13

Plain-language 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.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: \- Adults (age \>18yr) undergoing emergent endoscopy for active GI bleeding. Exclusion Criteria: * Patients with pre-existing heart failure (ejection fraction \<40%), cardiac rhythm abnormalities and peripheral vascular disease. * Patients with underlying implanted cardiac electrical devices and spinal cord stimulators.

What they're measuring

Changes in peripheral pulse volume with and without active bleeding

Timeframe: Baseline, approximately 2 hours post endoscopy

Trial details

NCT IDNCT06441201

SponsorMayo Clinic

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2025-09-22

View on ClinicalTrials.gov More GastroIntestinal Bleeding trials