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Low MAP Group for Traumatic Shock
N/A
Waitlist Available
Led By Matthew M Carrick, MD
Research Sponsored by Baylor College of Medicine
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
All adult patients seen in the Ben Taub emergency center that have suffered a trauma, have a systolic blood pressure less than 90mm Hg, and are going to the operating room for a laparotomy or thoracotomy
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 30 days
Awards & highlights
Study Summary
The goal of this study will be to determine if a lower than normal blood pressure during surgery for bleeding in the abdomen or chest will result in decreased bleeding and decreased chance of death.
Eligible Conditions
- Trauma
- Traumatic Shock
- Hemorrhagic Shock
- Multiple Trauma
- Penetrating Wounds
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 30 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~30 days
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
30 day survival
Secondary outcome measures
APACHE II
ARDS
Acidosis (pH and BE)
+11 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Low MAP GroupExperimental Treatment1 Intervention
Hypotensive Group with a target minimum MAP of 50 mmHg
Group II: High MAP groupActive Control1 Intervention
Non experimental group: These patients will have a target minimum MAP of 65 mm Hg
Find a Location
Who is running the clinical trial?
Baylor College of MedicineLead Sponsor
1,001 Previous Clinical Trials
6,002,141 Total Patients Enrolled
Matthew M Carrick, MDPrincipal InvestigatorBaylor College of Medicine
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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