Evaluation of Liver and Cardiometabolic Health Benefits on Low Carbohydrate Ketogenic Diet

Sponsor
Virginia Commonwealth University (Other)
Overall Status
Completed
CT.gov ID
NCT03141008
Collaborator
Obesity Treatment Foundation (Other)
54
1
29.4
1.8

Study Details

Study Description

Brief Summary

To evaluate the impact of a Low Carbohydrate Ketogenic Diet (LCKD) weight loss program and compare to the standard of care program established for patients with Non-Alcoholic Fatty Liver Disease (NAFLD) on: (1) Liver fat and liver stiffness scores, (2) lipid profile and insulin sensitivity; and (3) depression scores and quality of life, and (4) Cardiometabolic measures such as cardiopulmonary exercise test (CPET) and transthoracic echocardiogram (TTE).

Condition or Disease Intervention/Treatment Phase
  • Other: Fibroscan changes with different diets

Detailed Description

This prospective pilot pragmatic trial will investigate the role of a LCKD weight loss program for obese patients (BMI ≥30 kg/m2) and compare it to the group of known obese NAFLD patients who receive dietetic counseling as part of their standard of care in a dedicated NAFLD program. All participants (n=50) will be recruited at Virginia Commonwealth University (VCU).

Patients will do initial paperwork including

Questionnaires QOL, eating disorder screen, depression screen:

QOL, eating disorder screen and depression screen.

Labwork:

Data will be collected from routine care labwork to include a fasting cholesterol panel, insulin, A1c and comprehensive panel (if they have not received these labs in the preceding 3 months), and at 6 and 12 months. A1c will be collected at 3,6,9 months as well (if A1c >/=7), or just additionally at 6 months if A1c <7

Study labs will be collected:

Blood at 0, 3, 6 and 12 months Urine, stool and saliva at 0, 1, 3 and 12 months

Fibroscan will be done at 0, 3, 6 and 12 months

Echo/CPET testing and Room calorimetry will be offered and the patients agreeing to do this will have them done at 0, 3 and 12 months

Study Design

Study Type:
Observational
Actual Enrollment :
54 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Evaluation of Liver and Cardiometabolic Health Benefits on Low Carbohydrate Ketogenic Diet
Actual Study Start Date :
Sep 15, 2017
Actual Primary Completion Date :
Feb 27, 2020
Actual Study Completion Date :
Feb 27, 2020

Arms and Interventions

Arm Intervention/Treatment
Ketogenic diet exposed group

Fibroscan changes with different diets: Patients in a weight loss program using a ketogenic diet. Will compare differences in Fibroscan and metabolic changes.

Other: Fibroscan changes with different diets
Observational study of liver fat and stiffness and cardiometabolic parameters comparing two different standard of care dietary regimens

NAFLD diet exposed group

Fibroscan changes with different diets: Patients in a NAFLD clinic using low calorie, low fat diet. Will compare differences in Fibroscan and metabolic changes.

Other: Fibroscan changes with different diets
Observational study of liver fat and stiffness and cardiometabolic parameters comparing two different standard of care dietary regimens

Outcome Measures

Primary Outcome Measures

  1. Change in liver fat and stiffness scores compared to control group as well as intrasubject trend [0, 3, 6, 12 months]

    Performed with a fibroscan

Secondary Outcome Measures

  1. Change in Cardiometabolic labs [0, 6, 12 months (3 and 9 months for A1c if >7]

    Lipids, A1c, Insulin, comprehensive metabolic panel

  2. Other specialized testing [Only to a few of the eligible patients, 0, 3, 12 months]

    Echo, cardiopulmonary exercise testing, room calorimetry

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • The inclusion criteria include patients aged 18 years and older, BMI ≥ 30, ALT (alanine transferase) > 19 (female) and > 30 (male) or radiographic evidence of hepatic parenchymal disease and seen in either the PIs weight loss clinic or a patient in the VCU NAFLD (non-alcoholic fatty liver disease) program.
Exclusion Criteria:
  • Patients will be excluded if they have known other liver disease such as viral hepatitis, autoimmune hepatitis, liver transplant, severely ill, weekly alcohol use (>14 drinks in men and >7 drinks in women), HIV, pregnant females, those< 18 years, and prisoners.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Virginia Commonwealth University Richmond Virginia United States 23298

Sponsors and Collaborators

  • Virginia Commonwealth University
  • Obesity Treatment Foundation

Investigators

  • Principal Investigator: Susan Wolver, MD, VCU

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Virginia Commonwealth University
ClinicalTrials.gov Identifier:
NCT03141008
Other Study ID Numbers:
  • HM20009338
First Posted:
May 4, 2017
Last Update Posted:
Mar 10, 2020
Last Verified:
Mar 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Virginia Commonwealth University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 10, 2020