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Ketogenic Diet for Traumatic Brain Injury (KETI)

University of Missouri (MU) logo

University of Missouri (MU)

Status and phase

Completed
Early Phase 1

Conditions

Traumatic Brain Injury
Ketogenic Dieting

Treatments

Other: Ketogenic diet

Study type

Interventional

Funder types

Other

Identifiers

NCT03982602
2014675

Details and patient eligibility

About

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.

Full 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.

Enrollment

15 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Severe Traumatic Brain Injury
  2. GCS<= 8 with severe head injury
  3. Age more than 18years

Exclusion criteria

  1. Diabetic Ketoacidosis
  2. Unstable metabolic condition (persistent hyponatremia, hypernatremia, hypoglycemia, hypocalcemia, acidosis)
  3. Cardiorespiratory or hemodynamic instability
  4. Coagulopathy
  5. Pancreatitis
  6. Liver Failure
  7. Severe hyperlipidemia
  8. Inability to tolerate enteral feeds including ileus
  9. Known Fatty acid oxidation disorder or pyruvate carboxylase deficiency
  10. Any terminally ill patient with poor brain stem reflexes and mortality within 24h of admission.
  11. Pregnant Females

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

15 participants in 1 patient group

Subjects on Ketogenic diet
Experimental group
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.
Treatment:
Other: Ketogenic diet

Trial contacts and locations

1

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Central trial contact

Niraj Arora, MD

Data sourced from clinicaltrials.gov

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