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

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Enrolling

Conditions

Post Induction Hypotension

Treatments

Procedure: Group 1: LEE

Study type

Interventional

Funder types

Other

Identifiers

NCT06513169
HSC-MS-22-0145

Details and patient eligibility

About

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

Enrollment

200 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • American Society of Anesthesiologists (ASA)3 or lower
  • Patients requiring general anesthesia

Exclusion criteria

  • Allergic reaction to drugs commonly used for general anesthesia including fentanyl, midazolam, propofol, ephedrine and phenylephrine
  • Pregnant women
  • Requiring rapid sequence induction
  • Prisoners
  • Patient refusal
  • Emergency Surgery

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

200 participants in 2 patient groups

Group 1: LEE
Experimental group
Treatment:
Procedure: Group 1: LEE
Group 2: no LEE
No Intervention group

Trial contacts and locations

1

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Central trial contact

Erikka Washington; Ranganathan Govindaraj, MD

Data sourced from clinicaltrials.gov

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