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ClinicalTrials.gov public records Last synced Oct 30, 2026, 7:07 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Showing 1–21 of 21 matching trials from the live ClinicalTrials.gov search.

Filters: Condition: Resuscitation, Trauma Patients Clear all

Conditions: Congestive Heart Failure, Infections, Sepsis, Acute Renal Failure, Stroke
Interventions: Script and CPR/Mechanical ventilation video.; Other
Lead sponsor: Jewish Hospital, Cincinnati, Ohio; Other
Eligibility: 65 Years and older
Enrollment: 200 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2013 – 2014
U.S. locations: 1
States / cities: Cincinnati, Ohio

Conditions: Replacement of Supralaryngeal Airway
Interventions: replacing supralaryngeal airway with ET tube; Other
Lead sponsor: University of Wisconsin, Madison; Other
Eligibility: Male only
Enrollment: 50 participants
Healthy volunteers: Accepts healthy volunteers
Timeline: 2006 – 2010
U.S. locations: 1
States / cities: Madison, Wisconsin

Conditions: Critical Illness, Trauma
Interventions: Device: FloTrac™ and EV1000™, Volume Challenge, Vasopressor Therapy, Inotropic Therapy; Device · Other · Drug
Lead sponsor: CAMC Health System; Other
Eligibility: 18 Years and older
Enrollment: 48 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2015 – 2017
U.S. locations: 1
States / cities: Charleston, West Virginia

Conditions: Burns
Interventions: Not listed
Lead sponsor: University of North Carolina, Chapel Hill; Other
Eligibility: Not listed
Enrollment: 460 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2005 – 2008
U.S. locations: 11
States / cities: Phoenix, Arizona • San Francisco, California • Gainesville, Florida + 8 more

Conditions: Blunt Trauma, Penetrating Wound, Hemorrhagic Shock
Interventions: 0.9% Sodium Chloride 250 mL bolus, 0.9% Sodium Chloride 2000 mL bolus; Drug
Lead sponsor: University of Washington; Other
Eligibility: 15 Years and older
Enrollment: 192 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2012 – 2013
U.S. locations: 5
States / cities: Birmingham, Alabama • Portland, Oregon • Pittsburgh, Pennsylvania + 2 more

Conditions: Traumatic Brain Injury, Hemorrhagic Shock, Trauma
Interventions: Not listed
Lead sponsor: University of California, San Francisco; Other
Eligibility: 18 Years and older
Enrollment: 67 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2006 – 2011
U.S. locations: 1
States / cities: San Francisco, California

Conditions: Trauma
Interventions: Not listed
Lead sponsor: University of Miami; Other
Eligibility: 18 Years to 65 Years
Enrollment: 119 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2007 – 2010
U.S. locations: 1
States / cities: Miami, Florida

Conditions: Wounds and Injuries, Multiple Trauma, Disorder of Fluid Balance
Interventions: Plasmalyte A, Normal Saline; Other
Lead sponsor: University of California, Davis; Other
Eligibility: 18 Years and older
Enrollment: 46 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2011 – 2012
U.S. locations: 1
States / cities: Sacramento, California

Conditions: Resuscitation, Trauma Patients
Interventions: Not listed
Lead sponsor: University of California, San Francisco; Other
Eligibility: 1 Year to 90 Years
Enrollment: 60 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2010 – 2015
U.S. locations: 1
States / cities: San Francisco, California

Conditions: Hemorrhagic Shock, Trauma, Wounds, Penetrating, Shock, Traumatic, Multiple Trauma
Interventions: Intraoperative Hypotensive Resuscitation; Procedure
Lead sponsor: Baylor College of Medicine; Other
Eligibility: 12 Years to 45 Years
Enrollment: 271 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2007 – 2011
U.S. locations: 1
States / cities: Houston, Texas

Conditions: Septic Shock
Interventions: Plasma, Balanced crystalloids; Drug
Lead sponsor: The University of Texas Health Science Center, Houston; Other
Eligibility: 18 Years and older
Enrollment: 16 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2018 – 2019
U.S. locations: 1
States / cities: Houston, Texas

Conditions: Hemorrhagic Shock
Interventions: Glutamine, Ringer's Lactate, Placebo (for Glutamine); Drug
Lead sponsor: University of Missouri, Kansas City; Other
Eligibility: 21 Years to 65 Years
Enrollment: 5 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2011 – 2013
U.S. locations: 2
States / cities: Kansas City, Missouri

Conditions: Wound; Abdomen, Abdomen, Acute, Wound Surgical
Interventions: Abthera™ Open Abdomen Negative Pressure Therapy Device System, Dianeal PD-2 with 2.5% Dextrose; Device · Drug
Lead sponsor: Sanford Health; Other
Eligibility: 18 Years and older
Enrollment: 200 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2021 – 2026
U.S. locations: 1
States / cities: Fargo, North Dakota

Conditions: Traumatic Injury
Interventions: Galactose, Standard surgical methods; Procedure
Lead sponsor: University of Louisville; Other
Eligibility: 18 Years and older
Enrollment: 7 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2012 – 2016
U.S. locations: 1
States / cities: Louisville, Kentucky

Conditions: Cirrhosis, Liver, Acute Kidney Injury, Hepatorenal Syndrome
Interventions: Recommendation: No Further Resuscitation, Recommendation: Resuscitation with Crystalloid, Recommendation: Resuscitation with Colloid, Recommendation: Standard of Care IV Albumin; Other
Lead sponsor: Massachusetts General Hospital; Other
Eligibility: 18 Years and older
Enrollment: 50 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2024 – 2027
U.S. locations: 1
States / cities: Boston, Massachusetts

Conditions: Burns
Interventions: Intravenous Vitamin C, Vitamin C; Drug
Lead sponsor: United States Army Institute of Surgical Research; Federal
Eligibility: 18 Years to 72 Years
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2006 – 2008
U.S. locations: 1
States / cities: Fort Sam Houston, Texas

Conditions: Acute Coagulopathy
Interventions: Blood product transfusion based on conventional coagulation tests., Blood product transfusion based on rapid thrombelastography (r-TEG) results.; Biological
Lead sponsor: Denver Health and Hospital Authority; Other
Eligibility: 18 Years and older
Enrollment: 114 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2010 – 2014
U.S. locations: 1
States / cities: Denver, Colorado

Conditions: Trauma
Interventions: Thromboelastometry guided transfusion; Procedure
Lead sponsor: University of Texas Southwestern Medical Center; Other
Eligibility: 14 Years to 100 Years
Enrollment: 31 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2016 – 2018
U.S. locations: 1
States / cities: Dallas, Texas

Conditions: Critical Illness, Pediatrics, General Surgery, Fluid Therapy, Wounds and Injuries
Interventions: Balanced crystalloid solution volume administration, Packed Erythrocytes Units, Blood Product Unit volume, Plasma volume, Platelets volume; Other
Lead sponsor: Columbia University; Other
Eligibility: 6 Months to 15 Years
Enrollment: 250 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2018 – 2027
U.S. locations: 4
States / cities: Buffalo, New York • New York, New York • Rochester, New York + 1 more

Conditions: Patients Who Are in Shock and Intubated in the Trauma Bay (TB)
Interventions: Limited Transthoracic Echocardiogram (LTTE, SonoSite Ultrasound), Usual care; Device · Other
Lead sponsor: Riverside University Health System Medical Center; Other
Eligibility: 18 Years to 85 Years
Enrollment: 110 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2014 – 2018
U.S. locations: 1
States / cities: Moreno Valley, California

Conditions: C.Surgical Procedure; Cardiac
Interventions: Acute normovolemic hemodilution, Standard care; Procedure
Lead sponsor: Università Vita-Salute San Raffaele; Other
Eligibility: 18 Years and older
Enrollment: 2,000 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2019 – 2026
U.S. locations: 2
States / cities: Oklahoma City, Oklahoma • Charlottesville, Virginia

Search by objective public record fields.

Does Detailed Informed Consent for Cardiopulmonary Resuscitation and Mechanical Ventilation Impact Patients' Decisions and Outcomes?

Evaluation of Supralaryngeal Airway Removal During Initial Resuscitation of the Trauma Patient

Fluid Resuscitation Optimization in Surgical Trauma Patients (FROST)

Albumin Use in Burn Patients

Field Trial of Hypotensive Versus Standard Resuscitation for Hemorrhagic Shock After Trauma

The Use of Tissue Oxygen Monitoring in Critically Injured Patients

Optimal Fluid Resuscitation for Trauma Patients

Normal Saline Versus Plasmalyte in Initial Resuscitation of Trauma Patients

Early Aggressive Correction of Severe Acidosis With Tris-hydroxymethylaminomethane (THAM)

A Comparison of Two Target Mean Arterial Pressures in the Resuscitation of Hypotensive Trauma Patients

Resuscitation With Plasma in Surgical and Trauma Patients With Septic Shock

Biological Response of Trauma Patients to Standard Trauma Resuscitation Therapy

Direct Resuscitation of the Open Peritoneum

Direct Peritoneal Resuscitation Effects in the Damage Control Patient

Initial Resuscitation for Acute Kidney Injury in Cirrhosis

The Effect of High Dose Vitamin C in Burn Patients

Comparison of Rapid Thrombelastography and Conventional Coagulation Testing for Haemostatic Resuscitation in Trauma

Rotational Thromboelastometry Activated Transfusion In Trauma Trial

Effect of Giving Reduced Fluid in Children After Trauma

The Prognostic Value of Limited Transthoracic Echocardiogram (LTTE) During Trauma Resuscitation

Acute Normovolemic Hemodilution in High Risk Cardiac Surgery Patients.