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Saline irrigation for Blood Loss
N/A
Waitlist Available
Led By Arturo Cardounel, M.D.
Research Sponsored by Virginia Commonwealth University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 hours after the end of surgery
Awards & highlights
Study Summary
This trial will investigate if warmer temperatures during surgery reduces blood loss and clotting.
Eligible Conditions
- Blood Loss
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24 hours after the end of surgery
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 hours after the end of surgery
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Amount of blood loss
Chest temperature
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: ExperimentalExperimental Treatment1 Intervention
this cohort will receive 2 L of warm 37celsius saline irrigation of the mediastinum prior to closure of the chest
Group II: ControlActive Control1 Intervention
this cohort will receive the normal standard of care as established by the primary surgeon
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Saline irrigation
2019
Completed Phase 3
~240
Find a Location
Who is running the clinical trial?
Virginia Commonwealth UniversityLead Sponsor
697 Previous Clinical Trials
22,884,996 Total Patients Enrolled
Arturo Cardounel, M.D.Principal InvestigatorVirginia Commonwealth University
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