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Hypotension Prediction Index to Predict Epidural-labor Analgesia Induced Hypotension

Hypotension Clinical Trial

Official title:
Hypotension Prediction Index to Predict Epidural-labor Analgesia Induced Hypotension -- Pilot Study

Clinical Trial Summary

The purpose of this pilot trial is to examine the feasibility and ease of use of monitoring by ClearSight in laboring and delivering patients with the intent to compare time-to-treatment of hypotension between conventionally monitored patients (Group CM) and those receiving HPI (Group CM + HPI) monitoring by ClearSight, in a population of healthy laboring women who receive epidural analgesia.

Clinical Trial Description

In a prospective study, we will achieve the following aims: To determine the feasibility and ease of use of the ClearSight monitoring system in the labor-delivery room (LDR) in detecting and monitoring hypotensive events post-epidural labor analgesia placement. To compare the Time-to-Treatment of hypotensive events between the conventionally monitored patients (Group CM) and those receiving HPI (Group CM + HPI) monitoring by ClearSight. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05906368
Study type Interventional
Source University of Pittsburgh
Contact Amy Monroe, MPH, MBA
Phone 4126236382
Email monroeal@upmc.edu
Status Not yet recruiting
Phase N/A
Start date March 11, 2026
Completion date April 30, 2027
View Details
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