A Clinical Decision Support Trial to Reduce Intraoperative Hypotension

NCT04062994 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30000

Last updated 2024-03-06

No results posted yet for this study

Summary

The purpose of this study is to provide messages to providers if their patient is at high risk of developing intraoperative hypotension based on past medical history and co-morbidities preoperatively and minutes of hypotension intraoperatively.

Conditions

Interventions

BEHAVIORAL

Nudge to reduce intraoperative hypotension

Providers will be alerted if their patients are at high risk of hypotension or at increased risk of sequelae from hypotension. Intraoperatively, if patients have more than 10 minutes of hypotension an alert will be displayed on the screen.

Sponsors & Collaborators

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-09-28
Primary Completion
2019-10-05
Completion
2019-10-05

Countries

  • United States

Study Locations

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Entities

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 NCT04062994 on ClinicalTrials.gov