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Behavioural Intervention

Lower Body Elevation for Low Blood Pressure

N/A
Waitlist Available
Led By Ranganathan Govindaraj, MD
Research Sponsored by The University of Texas Health Science Center, Houston
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
American Society of Anesthesiologists (ASA) 3 or lower
Patients requiring general anesthesia
Must not have
Requiring rapid sequence induction
Patient refusal
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from start of anesthesia upto institution of positive pressure ventilation (about 5 minutes)
Awards & highlights
No Placebo-Only Group

Summary

This trial aims to see if raising the lower body will decrease the likelihood of low blood pressure after anesthesia, compare the use of certain medications between patients with raised lower body and those without, and assess if

Who is the study for?
This trial is for patients with a moderate or lower risk during anesthesia (ASA 3 or below) who need general anesthesia but aren't pregnant, allergic to common anesthetic drugs, requiring emergency surgery, rapid induction, or are prisoners.
What is being tested?
The study tests if raising the legs (LEE) can prevent low blood pressure after starting general anesthesia. It compares how often vasoactive drugs are used and checks if LEE affects cardiac output in patients with and without leg elevation.
What are the potential side effects?
Since this trial involves standard procedures for inducing general anesthesia, side effects may include typical reactions to these medications such as nausea, dizziness, or allergic responses in those not previously identified as allergic.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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My health is stable enough for surgery.
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I need general anesthesia for my treatment.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I need a fast-acting anesthesia for my procedure.
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I have chosen not to participate in certain treatments or procedures.
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I am allergic to common anesthesia drugs like fentanyl and propofol.
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I require emergency surgery.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from start of anesthesia upto institution of positive pressure ventilation (about 5 minutes)
This trial's timeline: 3 weeks for screening, Varies for treatment, and from start of anesthesia upto institution of positive pressure ventilation (about 5 minutes) for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Number of participants that demonstrate hypotension
Secondary study objectives
Number of participants that demonstrate Nadir blood pressure

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Group 1: LEEExperimental Treatment1 Intervention
Group II: Group 2: no LEEActive Control1 Intervention

Find a Location

Who is running the clinical trial?

The University of Texas Health Science Center, HoustonLead Sponsor
950 Previous Clinical Trials
344,845 Total Patients Enrolled
Ranganathan Govindaraj, MDPrincipal InvestigatorThe University of Texas Health Science Center, Houston
1 Previous Clinical Trials
30 Total Patients Enrolled
~133 spots leftby Nov 2025