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Terminated Phase 4 Interventional

Plasma Resuscitation Without Lung Injury

ClinicalTrials.gov ID: NCT04681638

Public ClinicalTrials.gov record NCT04681638. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 1, 2026, 5:36 PM EDT

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

Official title

Plasma Resuscitation withOut Lung Injury

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The treatment of patients with major burns requires resuscitation with massive amounts of fluid, typically a type of salt water that is given by vein. This frequently results in injury to vital organs, especially the lungs and kidneys, and even in death. In this study, the investigators propose to use plasma, a specially prepared blood product made from the liquid part of blood, that has undergone special treatment to reduce the risk of disease transmission. The aims include 1) reduce the amount of fluid given during the first 24 hours after a burn 2) reduce the incidence of lung injury and other complications related to the administration of funds and 3) determine if the blood product has any effect on inflammation. An overall decrease the amount of fluids that burn patients receive should decrease the potential for lung injury, decrease days in the hospital, and improve survival.

Study identification

NCT ID
NCT04681638
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Enrollment
13 participants

Conditions and interventions

Conditions

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 16, 2022
Primary completion
Jun 28, 2024
Completion
Sep 28, 2024
Last update posted
Jan 28, 2025

2022 – 2024

United States locations

U.S. sites
6
U.S. states
5
U.S. cities
6
Facility City State ZIP Site status
University of Alabama at Birmingham Burn Center Birmingham Alabama 35294
University of Maryland School of Medicine Baltimore Maryland 21201
Vanderbilt University Medical Center Nashville Tennessee 37232
U.S. Army Burn Center Fort Sam Houston Texas 78234-6315
University of Texas Medical Branch Galveston Texas 77555
University of Washington School of Medicine Seattle Washington 98104-2499

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04681638, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 28, 2025 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04681638 live on ClinicalTrials.gov.

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