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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT05350657
Other study ID # HSR210490
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date May 1, 2022
Est. completion date February 14, 2023

Study information

Verified date February 2023
Source University of Virginia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study seeks to assess the kidney health effects of short-term healthful ketogenic diet in young, overweight adults.10 overweight (BMI 25-30 kg/m2) adult participants (ages 20-40 years) without major chronic conditions including diabetes, kidney, cardiac, or liver disease will receive an isocaloric, high protein and low carbohydrate ketogenic diet for 2 weeks.


Description:

After baseline measures are taken, 10 overweight (BMI 25-30 kg/m2) young adult participants (ages 20-40 years) without major chronic conditions including diabetes, kidney, cardiac, or liver disease will receive an isocaloric, high protein and low carbohydrate ketogenic diet for 2 weeks. Each participant will consume one meal daily in the Diet and Nutrition (DAN) laboratory metabolic kitchen at the University of Virginia (UVA) and receive the remainder of the daily food allocation packed out to consume at home. Plate-waste method and NDS-R software will be used to measure food consumption (all served and packed-out foods and all uneaten and returned portions will be weighed). Weight, blood pressure and symptom surveys will be monitored at least 3 times a week. Fasting blood and 24 hour urine samples will performed at baseline and the end of each week. Stool for microbiota will be assess at baseline and end of study. Adherence will be confirmed with urinary biomarkers (e.g. urinary nitrogen) and point of care blood testing ketones. Differences in estimated glomerular filtration rate (GFR) determined from serum creatinine and cystatin C will be evaluated for each participant to assess magnitude of increase in GFR on the ketogenic diet. Over the past decade new panels of biomarkers have become available measuring glomerular permeability (urine albumin to creatinine ratio; UACR) and kidney injury and repair (IL-18, kidney injury molecule 1 [KIM-1], neutrophil gelatinase-associated lipocalin [NGAL], liver fatty acid type binding protein [L-FABP], tumor necrosis factor α [TNF-α, TNF receptor 1 and 2], transforming growth factor beta [TGF-β], human cartilage glycoprotein 39 [YKL-40], and monocyte chemoattractant protein 1 [MCP-1]). Change in UACR comparing the end of two weeks to baseline will be the primary outcome. Changes in other kidney injury markers will be assessed as secondary and exploratory outcomes. Additional exploratory outcomes will include urine metabolomics and stool 16S rRNA to characterize the gastrointestinal microbiota. Biosamples will be stored in a repository for future uses.


Recruitment information / eligibility

Status Terminated
Enrollment 5
Est. completion date February 14, 2023
Est. primary completion date February 14, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria: - Overweight (BMI 25-30 kg/m2) - Weight stable for last 4 weeks by self-report - Residing in the greater Charlottesville/Albemarle area for >6 months out of the last year - Normal kidney function at baseline, eGFR =60 ml/min/1.73m2 and UACR <30 mg/g at screening Exclusion Criteria: - History of major medical comorbidities by self-report (history of diabetes; diagnosed kidney disease; diagnosed gastrointestinal disorders including inflammatory bowel disease, gastric bypass, intestinal resection, celiac disease or other malabsorption; esophageal or other disorders limiting ability to swallow food) - Systolic blood pressure >160 or <100 at screening - Daily use of diuretics such as hydrochlorothiazide - Serum potassium <3.5 or >5.1 mEq/L at screening - Serum magnesium <1.6 mg/dL at screening - Serum sodium <135 or >149 mEq/L at screening - HbA1c > 6.5% at screening - Fasting plasma glucose > 126 mg/dL at screening - Pregnant or breastfeeding women (confirmed by spot urine at screening) - Inability to give written informed consent in English - Inability to walk up to 1 mile at a slow pace between buildings for study visits - Food allergies - Eating ketogenic or low carbohydrate diet over last 4 weeks - Blood ketones positive at screening - Intolerance or dislike of any study foods limiting adherence - Inability to attend daily visits - Vulnerable population such as direct reports or students of the investigators - Lack of access to refrigeration or equipment to safely reheat meals

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Ketogenic Diet
2 week isocaloric, high protein and low carbohydrate ketogenic diet

Locations

Country Name City State
United States University of Virginia Charlottesville Virginia

Sponsors (1)

Lead Sponsor Collaborator
University of Virginia

Country where clinical trial is conducted

United States, 

References & Publications (7)

Bostock ECS, Kirkby KC, Taylor BV, Hawrelak JA. Consumer Reports of "Keto Flu" Associated With the Ketogenic Diet. Front Nutr. 2020 Mar 13;7:20. doi: 10.3389/fnut.2020.00020. eCollection 2020. — View Citation

Buren J, Ericsson M, Damasceno NRT, Sjodin A. A Ketogenic Low-Carbohydrate High-Fat Diet Increases LDL Cholesterol in Healthy, Young, Normal-Weight Women: A Randomized Controlled Feeding Trial. Nutrients. 2021 Mar 2;13(3):814. doi: 10.3390/nu13030814. — View Citation

Cao J, Lei S, Wang X, Cheng S. The Effect of a Ketogenic Low-Carbohydrate, High-Fat Diet on Aerobic Capacity and Exercise Performance in Endurance Athletes: A Systematic Review and Meta-Analysis. Nutrients. 2021 Aug 23;13(8):2896. doi: 10.3390/nu13082896. — View Citation

Hall KD, Guo J, Courville AB, Boring J, Brychta R, Chen KY, Darcey V, Forde CG, Gharib AM, Gallagher I, Howard R, Joseph PV, Milley L, Ouwerkerk R, Raisinger K, Rozga I, Schick A, Stagliano M, Torres S, Walter M, Walter P, Yang S, Chung ST. Effect of a plant-based, low-fat diet versus an animal-based, ketogenic diet on ad libitum energy intake. Nat Med. 2021 Feb;27(2):344-353. doi: 10.1038/s41591-020-01209-1. Epub 2021 Jan 21. — View Citation

Ludwig DS, Willett WC, Volek JS, Neuhouser ML. Dietary fat: From foe to friend? Science. 2018 Nov 16;362(6416):764-770. doi: 10.1126/science.aau2096. — View Citation

Mitchell NS, Scialla JJ, Yancy WS Jr. Are low-carbohydrate diets safe in diabetic and nondiabetic chronic kidney disease? Ann N Y Acad Sci. 2020 Feb;1461(1):25-36. doi: 10.1111/nyas.13997. Epub 2019 Jan 15. — View Citation

Yancy WS Jr, Westman EC, McDuffie JR, Grambow SC, Jeffreys AS, Bolton J, Chalecki A, Oddone EZ. A randomized trial of a low-carbohydrate diet vs orlistat plus a low-fat diet for weight loss. Arch Intern Med. 2010 Jan 25;170(2):136-45. doi: 10.1001/archinternmed.2009.492. Erratum In: JAMA Intern Med. 2015 Mar;175(3):470. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Within-person change in MCP-1 comparing Day 15 to pre-intervention Exploratory and tested at nominal and false discovery rate (FDR)-adjusted p-values Day 0 and day 15 of the intervention
Other Within person change in urine metabolites comparing Day 15 to pre-intervention Exploratory and tested at nominal and false discovery rate (FDR)-adjusted p-values Day 0 and day 15 of the intervention
Other Within person change in microbiome composition by 16s rRNA sequencing comparing Day 15 to pre-intervention Exploratory and tested at nominal and false discovery rate (FDR)-adjusted p-values Day 0 and day 15 of the intervention
Primary Within-person change in UACR comparing Day 15 to pre-intervention Urine Albumin-Creatinine Ratio comparison tested at alpha 0.05 Day 0 and day 15 of the intervention
Secondary Within-person change in eGFR-Cr comparing Day 15 to pre-intervention Tested at alpha 0.0125, corrected (Bonferroni correction) for 4 overall outcomes. Due to very high correlation between different eGFR equations these are not corrected as independent tests Day 0 and day 15 of the intervention
Secondary Within-person change in eGFR-Cystatin comparing Day 15 to pre-intervention Tested at alpha 0.0125, corrected (Bonferroni correction) for 4 overall outcomes. Due to very high correlation between different eGFR equations these are not corrected as independent tests Day 0 and day 15 of the intervention
Secondary Within-person change in eGFR-Cr-and-Cystatin comparing Day 15 to pre-intervention Tested at alpha 0.0125, corrected (Bonferroni correction) for 4 overall outcomes. Due to very high correlation between different eGFR equations these are not corrected as independent tests Day 0 and day 15 of the intervention
Secondary Within-person change in urine KIM-1 comparing Day 15 to pre-intervention Tested at alpha 0.0125, corrected (Bonferroni correction) for 4 overall outcomes. Due to very high correlation between different eGFR equations these are not corrected as independent tests Day 0 and day 15 of the intervention
Secondary Within-person change in urine NGAL comparing Day 15 to pre-intervention Tested at alpha 0.0125, corrected (Bonferroni correction) for 4 overall outcomes. Due to very high correlation between different eGFR equations these are not corrected as independent tests Day 0 and day 15 of the intervention
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