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NCT06513169 · ClinicalTrials.gov registry record · NA

Lower Extremity Elevation to Minimize Hemodynamic Instability During Induction of General Anesthesia

A NA study, sponsored by The University of Texas Health Science Center, Houston.

Completed
Registry status
NA
Development phase
200
Enrollment target

NCT06513169 is a NA study that has completed, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 200 participants.

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The verdict

NCT06513169, a NA study, has completed, sponsored by The University of Texas Health Science Center, Houston.

COMPLETED
Registry status
NA
Development phase
200 participants
Enrollment target

Study Summary

The purpose of this study is to determine if lower extremity elevation (LEE) will reduce the incidence of postinduction hypotension, to compare the utilization of vasoactive medications after induction in patients with LEE and patients without LEE and to determine if LEE will increase measured cardiac output

Interventions

  • PROCEDURE Group 1: LEE

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2024-08-12
Est. Completion 2025-06-27
Phase NA

What the Registry Record Tells You About NCT06513169

The ClinicalTrials.gov registry entry for NCT06513169 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Group 1: LEE is the first listed.

NCT06513169 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT06513169 about?

NCT06513169 is a clinical study titled "Lower Extremity Elevation to Minimize Hemodynamic Instability During Induction of General Anesthesia". The purpose of this study is to determine if lower extremity elevation (LEE) will reduce the incidence of postinduction hypotension, to compare the utilization of vasoactive medications after induction in patients with LEE and patients without LEE and to determine if LEE will increase measured cardi...

What is the current status of trial NCT06513169?

This trial is currently completed. It is a NA study. The enrollment target is 200 participants. The study started on 2024-08-12. Estimated completion is 2025-06-27.

What interventions are being tested in trial NCT06513169?

The interventions under investigation include: Group 1: LEE (PROCEDURE).

Who is sponsoring clinical trial NCT06513169?

This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.