Ketogenic Diet for Traumatic Brain Injury (KETI)
Primary Purpose
Traumatic Brain Injury, Ketogenic Dieting
Status
Recruiting
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
Ketogenic diet
Sponsored by
About this trial
This is an interventional treatment trial for Traumatic Brain Injury
Eligibility Criteria
Inclusion Criteria:
- Severe Traumatic Brain Injury
- GCS<= 8 with severe head injury
- Age more than 18years
Exclusion Criteria:
- Diabetic Ketoacidosis
- Unstable metabolic condition (persistent hyponatremia, hypernatremia, hypoglycemia, hypocalcemia, acidosis)
- Cardiorespiratory or hemodynamic instability
- Coagulopathy
- Pancreatitis
- Liver Failure
- Severe hyperlipidemia
- Inability to tolerate enteral feeds including ileus
- Known Fatty acid oxidation disorder or pyruvate carboxylase deficiency
- Any terminally ill patient with poor brain stem reflexes and mortality within 24h of admission.
- Pregnant Females
Sites / Locations
- University of Missouri HospitalRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Subjects on Ketogenic diet
Arm Description
Treatment with KD will consist of 4:1 [fat]: [protein + carbohydrate] weight ratio. KD will be started as soon as the patient is ready for alimentation (while they are in neurocritical care unit). The rate of feeds will be calculated by trained dietician on service. Ketogenic diet will be continued during the entire length of ICU stay. Supplementation with vitamins, calcium and phosphorus will be done.
Outcomes
Primary Outcome Measures
Effect of Ketogenic Diet on Intracranial Pressure
Intracranial Pressure will be measured hourly and it will be trended daily.
Development of Ketosis in blood
Serum beta-hydroxybutyrate will be done alternate day to assess the level of ketosis in blood.
Excretion of Ketones in Urine
Urine Ketones will be measured alternate day to assess the level of ketosis
Secondary Outcome Measures
Evaluate change in the neurological exam
Neurological exam will be documented with Glasgow Coma Scale.
Evaluate subjects with gastro-intestinal adverse effects
Adverse effects like Diarrhea, vomiting, abdominal distension (ileus), abdominal tenderness will be monitored.
Evaluate subjects for muscle wasting
Urinary Nitrogen and urinary creatinine will be measured alternate day to look for muscle wasting.
Full Information
NCT ID
NCT03982602
First Posted
June 3, 2019
Last Updated
March 28, 2023
Sponsor
University of Missouri-Columbia
1. Study Identification
Unique Protocol Identification Number
NCT03982602
Brief Title
Ketogenic Diet for Traumatic Brain Injury
Acronym
KETI
Official Title
Safety and Feasibility of Ketogenic Diet for Traumatic Brain Injury Study Protocol
Study Type
Interventional
2. Study Status
Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 4, 2019 (Actual)
Primary Completion Date
December 30, 2023 (Anticipated)
Study Completion Date
December 30, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Missouri-Columbia
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Traumatic Brain Injury is a major health concern in United States. There is a un-met need to develop new therapeutic options for faster neuron recovery without causing significant side effects. The role of ketones in neuronal recovery has been studied and has been found to be useful in decreasing size of contusion. The present study aims to study the safety and feasibility profile of ketogenic diet.
Detailed Description
Traumatic Brain Injury (TBI) is a major health concern for United States contributing nearly one-third of injury-related deaths in United States. The Centers for Disease Control and Prevention (CDC) estimates that 1.7 million people in the United States sustain a TBI each year. It is responsible for significant disabilities and the total cost of productivity loss was estimated to be $76.5 billion in the United States in 2004.
Several animal models have demonstrated the effectiveness of ketones in brain injury to decrease the size of contusion, improving cortical ATP levels, reduced brain edema and cellular apoptosis. Ketones have been shown to be effective in neuromodulation in animal models. Evaluation of carbohydrate free diet has been done in traumatic brain injury patients and it was noted to not cause fluctuations in blood glucose. There is a need for safety and feasibility study of ketogenic diet in traumatic brain injury patients and to understand the effectiveness in neuromodulation in humans. The present study focuses on identifying the safety and feasibility of KD in traumatic brain injury patients.
This pilot project data will be utilized to design future randomized clinical trials. Based on the safety data, further trials will be conducted to evaluate the effectiveness of KD in traumatic brain injury patients and its effectiveness in controlling elevated intracranial pressure. It will open the avenue for consideration of new treatment option for intracranial pressure management and functional recovery. From a nutrition perspective, Ketogenic diet might become the standard of care for this patient population.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Traumatic Brain Injury, Ketogenic Dieting
7. Study Design
Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Subjects on Ketogenic diet
Arm Type
Experimental
Arm Description
Treatment with KD will consist of 4:1 [fat]: [protein + carbohydrate] weight ratio. KD will be started as soon as the patient is ready for alimentation (while they are in neurocritical care unit). The rate of feeds will be calculated by trained dietician on service. Ketogenic diet will be continued during the entire length of ICU stay. Supplementation with vitamins, calcium and phosphorus will be done.
Intervention Type
Other
Intervention Name(s)
Ketogenic diet
Other Intervention Name(s)
Ketovie
Intervention Description
Subjects will be provided with the Ketogenic diet in the form of tube feeds once the decision is made to start the patient on diet.
Primary Outcome Measure Information:
Title
Effect of Ketogenic Diet on Intracranial Pressure
Description
Intracranial Pressure will be measured hourly and it will be trended daily.
Time Frame
Baseline, till patient on KD (maximim 1 month)
Title
Development of Ketosis in blood
Description
Serum beta-hydroxybutyrate will be done alternate day to assess the level of ketosis in blood.
Time Frame
Baseline, till patient on KD ( maximum 1month)
Title
Excretion of Ketones in Urine
Description
Urine Ketones will be measured alternate day to assess the level of ketosis
Time Frame
Baseline, till patient on KD (maximum 1 month)
Secondary Outcome Measure Information:
Title
Evaluate change in the neurological exam
Description
Neurological exam will be documented with Glasgow Coma Scale.
Time Frame
Baseline, before discharge from ICU
Title
Evaluate subjects with gastro-intestinal adverse effects
Description
Adverse effects like Diarrhea, vomiting, abdominal distension (ileus), abdominal tenderness will be monitored.
Time Frame
Baseline, till patient on KD (Maximum 1month)
Title
Evaluate subjects for muscle wasting
Description
Urinary Nitrogen and urinary creatinine will be measured alternate day to look for muscle wasting.
Time Frame
Baseline, till patient on Kd (Maximum 1month)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Severe Traumatic Brain Injury
GCS<= 8 with severe head injury
Age more than 18years
Exclusion Criteria:
Diabetic Ketoacidosis
Unstable metabolic condition (persistent hyponatremia, hypernatremia, hypoglycemia, hypocalcemia, acidosis)
Cardiorespiratory or hemodynamic instability
Coagulopathy
Pancreatitis
Liver Failure
Severe hyperlipidemia
Inability to tolerate enteral feeds including ileus
Known Fatty acid oxidation disorder or pyruvate carboxylase deficiency
Any terminally ill patient with poor brain stem reflexes and mortality within 24h of admission.
Pregnant Females
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Niraj Arora, MD
Phone
2672707551
Email
arorana@health.missouri.edu
Facility Information:
Facility Name
University of Missouri Hospital
City
Columbia
State/Province
Missouri
ZIP/Postal Code
65212
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Niraj Arora, MD
Phone
573-884-7975
Ext
5738829500
Email
arorana@health.missouri.edu
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
35063224
Citation
Arora N, Litofsky NS, Golzy M, Aneja R, Staudenmyer D, Qualls K, Patil S. Phase I single center trial of ketogenic diet for adults with traumatic brain injury. Clin Nutr ESPEN. 2022 Feb;47:339-345. doi: 10.1016/j.clnesp.2021.11.015. Epub 2021 Nov 16.
Results Reference
derived
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Ketogenic Diet for Traumatic Brain Injury
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