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Ketogenic Diet Following Moderate to Severe Pediatric Traumatic Brain Injury

Ketogenic Diet Following Moderate to Severe Pediatric Traumatic Brain Injury: A Pilot Study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04933448
Enrollment
7
Registered
2021-06-21
Start date
2022-05-16
Completion date
2024-12-31
Last updated
2026-02-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Traumatic Brain Injury

Brief summary

The primary objective of this study is to evaluate the feasibility and safety of using the ketogenic diet (KD) in children who sustained moderate to severe traumatic brain injury (TBI). The secondary objective is a preliminary evaluation of the outcomes of children who have had the standard of care plus the KD, compared to those with standard of care alone. Outcome measures for the secondary objective will include: need for ventriculoperitoneal shunt, duration of unconsciousness, need for any type of craniotomy, duration of post-traumatic amnesia, acute hospitalization length of stay, and cognitive and motor function at 12 months after injury. If this study demonstrates feasibility and safety, the information related to outcomes will be used to inform the planning of a future, larger, randomized study of the efficacy of the KD in children and adolescents with TBI. Specifically, this information will be used to assist with sample size calculations for this future study.

Detailed description

The KD is an alternative feeding regimen that has been in use since 1921. It is a high fat, low carbohydrate and moderate protein diet. There are various forms of the KD. The classic KD consists of long-chain triglycerides with a fat-to-combined-protein-and-carbohydrate ratio that can vary. At our institution, it is standard of care to initiate a ketogenic diet at a ratio of 2:1, and to increase the ratio to 3:1 or 4:1 as needed to achieve ketosis. Clinically, the KD has been proven to be an effective therapy in children and adolescents with refractory epilepsy, as well as for those with type II diabetes. In addition, an international consensus was published in 2009 that recommended the use of the KD to treat epilepsy refractory as an alternative to at least two antiepileptic medications. Before initiating the KD for epilepsy management, labs such as urine and blood ketones, blood glucose and a basic metabolic panel including magnesium are commonly recommended. Risks for long-term use of the KD include but are not limited to the following: hypercholesterolemia, mineral deficiencies, acidosis, constipation, weight loss and nephrolithiasis. However, short-term use should significantly limit the occurrence of these potential complications.

Interventions

OTHERKetogenic Diet

The ketogenic diet (KD) is an alternative feeding regimen that has been in use since 1921. It is a high-fat, low carbohydrate, and moderate protein diet. There are various forms of the KD. The classic KD consists of long-chain triglycerides with a fat-to-combined-protein-and-carbohydrate ratio that can vary. At the investigating institution, it is standard of care to initiate a ketogenic diet at a ratio of 2:1, and to increase the ratio to 3:1 or 4:1 as needed to achieve ketosis.

Sponsors

Gillette Children's Specialty Healthcare
Lead SponsorOTHER
State of Minnesota Spinal Cord Injury and Traumatic Brain Injury Research Grant Program
CollaboratorUNKNOWN

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
2 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* Age limits met at the time of injury and admission * Participants with moderate to severe traumatic brain injury defined as a Glasgow Coma Scale Score of 3-12 (lowest score in the first 24 hours after injury). Individuals requiring craniotomy and/or evacuation of intracranial hemorrhage may be included.

Exclusion criteria

* Currently on an oral diet at time of screening or currently on IV-only and in opinion of Pediatric Intensive Care Unit intensivist will be transitioning to an oral diet, not tube-feeding * Anoxia/ischemia as a significant portion of injury, including near-drowning * Non-accidental traumatic brain injury (i.e., assault, abuse) * Penetrating injury including gunshot wounds * Pregnancy * Any condition that in the opinion of the Pediatric Intensive Care Unit or neurosurgery medical staff warrants exclusion from the study

Design outcomes

Primary

MeasureTime frameDescription
Ability to complete a course of the ketogenic diet (KD)14 daysSafety and feasibility will be determined by the ability to complete a 14-day course of the KD after TBI without needing to terminate the diet due to intolerance resulting from gastrointestinal side effects (for example, nausea and vomiting, diarrhea, or acidosis), or due to abnormal findings on laboratory tests. Outcome is reported as the number of participants who complete the 14-day keto diet treatment.

Secondary

MeasureTime frameDescription
Duration of Unconsciousness14 daysOutcome is reported as the length of time (in hours) a participant is unconscious following their injury.
Need for Surgeries14 daysOutcome is reported as the number of surgeries required in each group following injury.
Duration of Acute Hospitalization14 daysOutcome is reported as the length (in days) of acute hospitalization following injury.
Duration of Post-traumatic Amnesia14 daysOutcome is reported as the length of time (in days) that a participant experiences amnesia following their injury.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORLinda Krach, MD

Department of Physical Medicine and Rehabilitation

PRINCIPAL_INVESTIGATORAngela Sinner, DO

Department of Physical Medicine and Rehabilitation

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026