Oral Rehydration Therapy in Burn Patients
NCT02124265 · Status: TERMINATED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 3
Last updated 2019-02-18
Summary
In patients with moderate to severe thermal injuries (\> 20% TBSA) adequate fluid resuscitation is the main priority to achieve successful outcomes. Soon after burn injury substantial amounts of fluid accumulate rapidly in the wound while more is lost in the third space. Without intervention this process leads to hypotension and shock. The Parkland formula was devised to calculate how much intravenous (IV) fluid, i.e. crystalloids, is needed for adequate resuscitation during the first 24 hours post-burn. However, IV resuscitation can lead to overexpansion of (third space) volume, leading to severe complications such as compartment syndrome or pulmonary edema.
In major population centers, catastrophic events causing mass casualties will disrupt many hospital and emergency services, potentially delaying acute IV fluid resuscitation. Burn patient case reports have shown that oral rehydration therapy (ORT) used to supplement or in place of IV therapy is efficacious. ORT could be easily applied in mass burn casualties.
ORT is generally known in the third world for treating life-threatening dehydration due to diarrhea. The glucose-sodium co transport mechanism enables the affected human intestine to absorb a sufficient amount of water and electrolytes to replace large fluid losses due to severe diarrhea, even under adverse field conditions. No electrolyte disturbances have been recorded in such cases. Studies on enteral resuscitation in animal burn models showed high rates of small intestinal absorption which should be adequate for resuscitation following major burn injury.
The optimal composition of oral rehydration solution for resuscitation in burn wounds has not been determined. In cholera patients, Ceralyte® has proven superior to the World Health Organization Oral Rehydration Solution, increasing fluid absorption of the intestine. The Ceralyte® 90 solution, with 90mEq/L sodium and a low osmolarity of \<275mOsm, may also contribute to optimal intestinal fluid uptake without causing electrolyte disturbances in thermal injury. ORT use might reduce the occurrence of compartment syndrome and pulmonary edema since fluid is regulated by the intestine according to physiologic requirements. The investigators propose to conduct a prospective study using Ceralyte® 90 to show that oral resuscitation therapy (ORT) in burns can reduce the total amount of IV fluid needed for adequate resuscitation and to test the efficacy and safety of ORT in the resuscitation of burn patients.
Conditions
- Burn Any Degree Involving 20-29 Percent of Body Surface
- Burn Any Degree Involving 30-39 Percent of Body Surface
- Burn Any Degree Involving 40-49 Percent of Body Surface
- Burn Any Degree Involving 50-59 Percent of Body Surface
- Burn Any Degree Involving 60-65 Percent of Body Surface
- Fluid Resuscitation
Interventions
- DRUG
-
CeraLyte 90
1. This is a prospective pilot study of patients with moderate-major burn wounds (20-65% TBSA). 2. Patients who meet inclusion/exclusion criteria will be enrolled in the study upon admission to the Burn Unit. 3. Fluid requirements will be calculated according to the Parkland Formula (4 cc/kg/% Total Body Surface Area) administered over 24 hours since time of injury. 5\. Patients will be monitored according to standard of care. a. If gastric residuals are \>300cc, ORT will be stopped and only IV fluid resuscitation will be used.
Sponsors & Collaborators
- lead OTHER
Principal Investigators
-
Stephen M Milner, MBBS · Johns Hopkins University
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-05-31
- Primary Completion
- 2015-03-31
- Completion
- 2015-03-31
- FDA Drug
- Yes
Countries
- United States
Study Locations
More Related Trials
-
Optimizing Fluid Resuscitation in Adults With Major Burns: A Randomized Trial of Burn Navigator™ Versus Parkland Formula
NCT07307599 ·Status: NOT_YET_RECRUITING ·Phase: PHASE4
-
Patient Controlled Fluid Administration
NCT03176043 ·Status: UNKNOWN ·Phase: EARLY_PHASE1
-
Plasma Resuscitation Without Lung Injury
NCT04681638 ·Status: TERMINATED ·Phase: PHASE4
-
Oral Rehydration Solution in Healthy Adults
NCT06130475 ·Status: COMPLETED ·Phase: NA
-
Safety Study of Inhaled Saline in Acute Lung Injury
NCT01713595 ·Status: WITHDRAWN ·Phase: PHASE1
-
Fluid Shifts During Resuscitation: Impacts on Macrocirculation and Microcirculation
NCT00326729 ·Status: UNKNOWN
-
A Comparison of Three Commercial Oral Rehydration Solutions Consumed After Extra-cellular Dehydration
NCT05775055 ·Status: COMPLETED ·Phase: NA
-
Feasibility and Safety of Delivering a Ketone Drink to Comatose Survivors of Out-of-hospital Cardiac Arrest
NCT03226197 ·Status: COMPLETED ·Phase: NA
-
Descriptive Study of Cardiac Output During Rehydration With Recombinant Human Hyaluronidase in Pediatrics
NCT01139294 ·Status: COMPLETED ·Phase: PHASE4
-
Water Deprivation Protocol
NCT01224704 ·Status: COMPLETED ·Phase: NA
-
The Acute Burn Resuscitation Multicenter Prospective Observational Trial
NCT03144427 ·Status: COMPLETED
-
Relieve the Patient's Thirst, Refresh the Mouth First (ICU-MIC)
NCT03610074 ·Status: COMPLETED ·Phase: NA
-
IV NaCl (Sodium Chloride) 0.9% Vs (Versus) IV NaCl 0.9% + 5% Dextrose in Pediatric ER for Dehydration
NCT02054585 ·Status: UNKNOWN ·Phase: NA
-
Rehydration Efficiency During Ad-libitum Fluid Intake
NCT06414291 ·Status: COMPLETED ·Phase: NA
-
Oral Fluid Volume Expansion
NCT01360333 ·Status: COMPLETED ·Phase: NA
-
Albumin and Prognosis of Severely Patients Burns
NCT04264065 ·Status: RECRUITING
-
Hypertonic Resuscitation Following Traumatic Injury
NCT00316017 ·Status: TERMINATED ·Phase: PHASE3
-
Treatment With the Ketone Body 3-hydroxybutyrate in Patients With Cardiogenic Shock
NCT04642768 ·Status: COMPLETED ·Phase: NA
-
Hypertonic Saline With Dextran for Treating Hypovolemic Shock and Severe Brain Injury
NCT00113685 ·Status: COMPLETED ·Phase: NA
-
The Effect of AMP Human Sodium Bicarbonate Lotion on Dehydrated Heat Stress
NCT05092854 ·Status: COMPLETED ·Phase: NA
-
Fluid Resuscitation With HES 200/0.5 10% in Severe Burn Injury
NCT01120730 ·Status: COMPLETED ·Phase: PHASE3
-
Hypertonic Saline for Fluid Resuscitation After Cardiac Surgery
NCT03280745 ·Status: COMPLETED ·Phase: PHASE4
-
Physiological Effects of 38°C vs. 22°C Fluid Therapy in Critically Ill Patients
NCT04576806 ·Status: WITHDRAWN ·Phase: NA
-
Effect of Nebulized and Intravenous Hypertonic Saline 3% on the Management of Patients With Acute Respiratory Distress Syndrome
NCT06226402 ·Status: RECRUITING ·Phase: NA
-
A Prospective Observational Study of the Expectations and Physiological Effects of Fluid Bolus Therapy
NCT03178578 ·Status: UNKNOWN