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Ketogenic Diet to Improve Neuro-recovery

Primary Purpose

Spinal Cord Injuries

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Ketogenic Diet
Standard Diet
Sponsored by
Ohio State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Spinal Cord Injuries

Eligibility Criteria

19 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Clinically motor complete and incomplete spinal cord injury, age 19-60
  • ASIA A, B, C or D (ASIA: Neurological Impairment Scale)

Exclusion Criteria:

  • Pregnant women.
  • Neurological (other than SCI), vascular and/or cardiac problems that may limit function and interfere with testing procedures
  • Patients with evidence of renal insufficiency and liver disease by history, physical examination, and laboratory tests
  • Patients with underlying pulmonary diseases

Sites / Locations

  • Ohio State University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Ketogenic Diet Group

Standard Diet Group

Arm Description

Ketogenic diet is a high-fat, low-carbohydrate diet (lipid to carbohydrate + protein ratio of 3:1) that included ≈72% total energy as fat, ≈25% as protein, and ≈3% as carbohydrate during enteral feeding and ≈65% total energy as fat, ≈27% as protein, and ≈8% as carbohydrate and fiber during solid feeding. Patients will start receiving ketogenic diet within the 72 hours injury, after completing their baseline measurements.

Patients will start to receive standard hospital diet within 72 hours of injury after completing their baseline measurements. Standard diet includes ≈35% total energy as fat, ≈27% as protein, and ≈44% as carbohydrate and fiber.

Outcomes

Primary Outcome Measures

Change in sensory and motor function
The ASIA Motor Index Score will be used for measuring motor function. This index uses standard manual muscle testing on a six grade scale. The total possible score from upper and lower extremity is 50. For the sensory examination, each dermatome will be tested for both sharp (pin-prick) and light-touch sensation and will be graded on a three point scale. Numerically, the sensory scores total 116 points. Measurement of motor and sensory function will take about an hour and will be performed 3 times during the course of the study.

Secondary Outcome Measures

Change in serum glucose concentration
Oral glucose tolerance test will be given to measure serum glucose concentration (mg/dl) after overnight fasting.
Change in functional Independence
The Spinal Cord Independence Measure (SCIM) will be used for measuring functional independence. The SCIM is, at present, the only comprehensive rating scale that measures the ability of patients with SCI to perform everyday tasks according to their value for the patient. It requires no manual testing and the range of the total score is 0 to 100.
Change in serum biomarkers for neurorecovery
Targeted proteomics analysis in serum samples will be used to quantify proteins and peptides known to be involved in neuro-inflammation in the acute stages of spinal cord injury including fibrinogen, extracellular signal-regulated kinase, ½, CD11b/CD18 integrin receptor, and epidermal growth factor receptor.
Change in serum insulin concentration
Oral glucose tolerance test will be given to measure serum insulin concentration (μU/ml ) after overnight fasting.

Full Information

First Posted
April 9, 2018
Last Updated
March 23, 2023
Sponsor
Ohio State University
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1. Study Identification

Unique Protocol Identification Number
NCT03509571
Brief Title
Ketogenic Diet to Improve Neuro-recovery
Official Title
Evaluation of a Ketogenic Diet for Improvement of Neurological Recovery in Individuals With Acute Spinal Cord Injury
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 9, 2019 (Actual)
Primary Completion Date
February 1, 2024 (Anticipated)
Study Completion Date
February 28, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ohio State University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this project is to determine if 5 weeks of ketogenic (KD, high-fat) diet vs. standard diet (SD) significantly improves motor and sensory function, glycemic function, and functional independence in patients with spinal cord injury.
Detailed Description
There is an urgent need for innovative therapies for improving neurorecovery after spinal cord injury (SCI). Despite extensive research, clinical advancements, and improved rehabilitation strategies, SCI continues to be a significant cause of disability and mortality. After a primary impact, the injured spinal cord undergoes multiple secondary pathological states that represent an important target in developing neuroprotective strategies for treatment of SCI. Even minor improvements in neurological recovery can have profound impacts on management of daily activities, secondary health complications, and quality of life. Thus, timely and effective strategies are of critical importance for positive outcomes after SCI. A number of pharmacological neuroprotective agents have been subject to intensive investigation in large, multicenter, prospective randomized controlled trials. Despite promising preclinical animal data, the primary outcomes of these clinical trials were largely negative. There is thus clear reason for researchers, clinicians, and patients to seek alternative therapies to enhance neurorecovery and functional status after SCI. The scientific premise of this project rests upon accumulating evidence that diet-based therapies, such as the ketogenic diet (KD), offer effective neuroprotection against secondary injury cascades and improve forelimb motor function in a rat model of SCI and improve upper extremity motor function in patients with acute SCI. The KD is a high-fat, low-carbohydrate diet designed to mimic the metabolic and biochemical changes that occur during calorie restriction, specifically ketosis. Ketone bodies have been shown to exert neuroprotective effects by preventing oxidative damage; attenuating neuroinflammation and glutamate excitotoxicity; and inhibiting apoptosis in the brain and spinal cord. Because glutamate excitotoxicity, inflammation, and induction of apoptotic pathways lead to progressive degeneration in the spinal cord shortly after the injury, inhibition of these processes by ketone bodies may enhance neurological recovery after an SCI. In support of these hypotheses, we recently showed for the first time that, compared with a standard hospital diet (SD), 5 weeks of KD improved upper extremity motor function in patients with acute SCI. In addition, a neuroinflammatory blood protein, fibrinogen, was present at lower levels in the KD serum samples than in the SD serum samples. Taken together, our results suggest that a KD may induce anti-inflammatory effects in part by reducing fibrinogen, which promotes neuroprotection and improved recovery. The acute stage post-SCI is also characterized by hyperglycemia, which is strongly associated with poor functional outcomes at discharge. These findings support the importance of achieving tight glycemic control in acute human SCI to obtain better neurological outcomes. Emerging evidence suggests that a KD can also improve the patient's metabolic state and maintain normal glycemic levels. In contrast, standard hospital diets have traditionally promoted a relatively high carbohydrate nutritional content. Consistent with previous findings, we have recently shown that 5 weeks of KD decreased fasting serum glucose levels by 24 mg/dl whereas levels increased by 0.7 mg/dl in the SD group. These provocative findings have led us to our central hypothesis that SCI patients who consume a KD over the first 5 weeks (average hospital stay) after injury will have better neurological recovery, functional independence, and glycemic control than the SCI patients who consume an SD during this period.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spinal Cord Injuries

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Ketogenic Diet Group
Arm Type
Experimental
Arm Description
Ketogenic diet is a high-fat, low-carbohydrate diet (lipid to carbohydrate + protein ratio of 3:1) that included ≈72% total energy as fat, ≈25% as protein, and ≈3% as carbohydrate during enteral feeding and ≈65% total energy as fat, ≈27% as protein, and ≈8% as carbohydrate and fiber during solid feeding. Patients will start receiving ketogenic diet within the 72 hours injury, after completing their baseline measurements.
Arm Title
Standard Diet Group
Arm Type
Other
Arm Description
Patients will start to receive standard hospital diet within 72 hours of injury after completing their baseline measurements. Standard diet includes ≈35% total energy as fat, ≈27% as protein, and ≈44% as carbohydrate and fiber.
Intervention Type
Other
Intervention Name(s)
Ketogenic Diet
Intervention Description
Enteral feeding via nasogastric (NG) or nasojejunal (NJ) tubes with ketogenic diet will start within 72 hours of injury and solid feeding will start as soon as the patient is able to swallow. This diet is a high-fat, low-carbohydrate diet (lipid to carbohydrate + protein ratio of 3:1) that will include ≈75% total energy as fat, ≈20% as protein, and ≈5% as carbohydrate and fiber.
Intervention Type
Other
Intervention Name(s)
Standard Diet
Intervention Description
Enteral feeding via nasogastric (NG) or nasojejunal (NJ) tubes with SD diet will start within 72 hours of injury and solid feeding will start as soon as the patient is able to swallow. This diet includes ≈35% total energy as fat, ≈27% as protein, and ≈44% as carbohydrate and fiber.
Primary Outcome Measure Information:
Title
Change in sensory and motor function
Description
The ASIA Motor Index Score will be used for measuring motor function. This index uses standard manual muscle testing on a six grade scale. The total possible score from upper and lower extremity is 50. For the sensory examination, each dermatome will be tested for both sharp (pin-prick) and light-touch sensation and will be graded on a three point scale. Numerically, the sensory scores total 116 points. Measurement of motor and sensory function will take about an hour and will be performed 3 times during the course of the study.
Time Frame
Baseline (within 72 hours of injury), 3 and 5 weeks
Secondary Outcome Measure Information:
Title
Change in serum glucose concentration
Description
Oral glucose tolerance test will be given to measure serum glucose concentration (mg/dl) after overnight fasting.
Time Frame
Baseline (within 72 hours of injury), 3 and 5 weeks
Title
Change in functional Independence
Description
The Spinal Cord Independence Measure (SCIM) will be used for measuring functional independence. The SCIM is, at present, the only comprehensive rating scale that measures the ability of patients with SCI to perform everyday tasks according to their value for the patient. It requires no manual testing and the range of the total score is 0 to 100.
Time Frame
Baseline (within 72 hours of injury), 3 and 5 weeks
Title
Change in serum biomarkers for neurorecovery
Description
Targeted proteomics analysis in serum samples will be used to quantify proteins and peptides known to be involved in neuro-inflammation in the acute stages of spinal cord injury including fibrinogen, extracellular signal-regulated kinase, ½, CD11b/CD18 integrin receptor, and epidermal growth factor receptor.
Time Frame
Baseline (within 72 hours of injury), 3 and 5 weeks
Title
Change in serum insulin concentration
Description
Oral glucose tolerance test will be given to measure serum insulin concentration (μU/ml ) after overnight fasting.
Time Frame
Baseline (within 72 hours of injury), 3 and 5 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinically motor complete and incomplete spinal cord injury, age 19-60 ASIA A, B, C or D (ASIA: Neurological Impairment Scale) Exclusion Criteria: Pregnant women. Neurological (other than SCI), vascular and/or cardiac problems that may limit function and interfere with testing procedures Patients with evidence of renal insufficiency and liver disease by history, physical examination, and laboratory tests Patients with underlying pulmonary diseases
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ceren Yarar-Fisher, PhD
Phone
205-977-0891
Email
yarar-fisher.1@osu.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Raquel Minarsch, DPT
Phone
330-881-1710
Email
raquel.minarsch@osumc.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ceren Yarar-Fisher, PhD
Organizational Affiliation
Ohio State University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Raquel Minarsch, DPT
Organizational Affiliation
Ohio State University
Official's Role
Study Director
Facility Information:
Facility Name
Ohio State University Hospital
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ceren Yarar-Fisher, PhD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32366293
Citation
Demirel A, Li J, Morrow C, Barnes S, Jansen J, Gower B, Kirksey K, Redden D, Yarar-Fisher C. Evaluation of a ketogenic diet for improvement of neurological recovery in individuals with acute spinal cord injury: study protocol for a randomized controlled trial. Trials. 2020 May 4;21(1):372. doi: 10.1186/s13063-020-04273-7.
Results Reference
derived

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Ketogenic Diet to Improve Neuro-recovery

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