Your session is about to expire
← Back to Search
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 belowSelect...
My health is stable enough for surgery.
Select...
I need general anesthesia for my treatment.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I need a fast-acting anesthesia for my procedure.
Select...
I have chosen not to participate in certain treatments or procedures.
Select...
I am allergic to common anesthesia drugs like fentanyl and propofol.
Select...
I require emergency surgery.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ from start of anesthesia upto institution of positive pressure ventilation (about 5 minutes)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from start of anesthesia upto institution of positive pressure ventilation (about 5 minutes)
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
Share this study with friends
Copy Link
Messenger