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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05767177
Other study ID # Ketogen05
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 1, 2023
Est. completion date December 31, 2025

Study information

Verified date September 2023
Source Göteborg University
Contact Lars Fändriks, MD, PhD
Phone +4631 3424123
Email lars.fandriks@gastro.gu.se
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this cross-over study in obese subjects is to learn about the common co-morbidity type 2 diabetes and the local formation of ketone bodies. The type of study is an exploratory trial with the participants as own controls. The main questions it aims to answer are: 1. Does food intake-induced ketogenesis exist in the small intestine of obese individuals? 2. Are insulin resistance, the incretin GLP-1 release and the glucose transporter SGLT1 affected in obese individuals without type 2 diabetes in the same way as those with type 2 diabetes?


Description:

The investigators have recently shown that the mucosa in the middle small intestine, the jejunum, in human volunteers produce ketones bodies.This situation is thus contrary to the common view that ketone bodies are formed by the liver during fasting/starvation. Obesity is commonly associated with hyperglycaemic conditions and diabetes mellitus type 2.This has given rise to the question of whether obesity results in disturbances in the intestinal food-induced ketogenesis and whether this influence contributes to the development of type 2 diabetes mellitus? The project's questions are therefore: 1. Does food intake-induced ketogenesis exist in the small intestine of obese individuals? 2. Are insulin resistance, the incretin GLP-1 release and the glucose transporter SGLT1 affected in obese individuals without type 2 diabetes in the same way as those with type 2 diabetes? 3. If no to 2: What is the difference?


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date December 31, 2025
Est. primary completion date July 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - BMI 35 to 45 kg/m2 Exclusion Criteria: - Insulin-treated diabetes - Sequelae of previous diabetes-associated disease (foot, eyes and kidneys, or cardiovascular incident, etc.) - Diabetes, hypertension, lipid disorder that has not been stabilized for at least 1 month by adequate pharmacological treatment - Continuous NSAID use - Preferably otherwise medication-free (exceptions can be made) - Not operated on in the abdomen (appendectomy excluded) - Previously known organic gastrointestinal disease, except for gastroesophageal reflux disease (GERD) - Smokers - Pregnancy and breastfeeding - History of drug abuse or other circumstances deemed to jeopardize the patient's ability to participate in the research project

Study Design


Intervention

Other:
Glucemia following Mixed Meal Test
On day 12 of each diet, a venous catheter is placed in one arm for blood sampling and the research person must answer questions about any gastrointestinal complaints in connection with the current diet. At approximately 09:00, the research subject may eat a brunch for approximately 15 minutes (sandwich, juice, fried egg and sausage; 550-600kcal). Venous blood samples are taken before and 15, 30, 45, 60, 90 and 120 minutes after the meal.
Enteroscopy - mucosal ketogenic activity as well as glucose transport
On day 14 of each diet period, an enteroscopy is performed. This step is performed to obtain samples (biopsy) of the mucosa of the small intestine (duodenum and jejunum) and is performed at the Gastro-endoscopic departments SU-Sahlgrenska, or SU-Eastern hospital. Endoscopy is experienced by some individuals as unpleasant, which is why local anesthesia and sometimes sedation (midazolam + pethidine or rapifen) can be offered according to standard routine in the endoscopy department.

Locations

Country Name City State
Sweden Dept of Surgery, Sahlgrenska Universityhospital Gothenburg

Sponsors (1)

Lead Sponsor Collaborator
Göteborg University

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Other Glucemia, insulinemia and GLPi-emia following the Mixed Meal Test The study participant arrives fasted and a venous catheter is placed in one arm for blood sampling. The research subject may eat a brunch for approximately 15 minutes (Mixed Meal Test (MMT): sandwich, juice, fried egg and sausage; 550-600kcal) and the p-glucose (mM), p-insulin (µUnits/mL) and p-GLP1 (pM) is checked after 15, 30, 45, 60, 90 and120 min.
The aggregated responses to MMT (linear area under the curve minus the baseline value) over 120 min of the respective agent are compared in high-carbohydrate diet and high-fad diet.
On day 12 of the respective diet
Primary Glucemia following a Mixed Meal Test: The study participant arrives fasted and a venous catheter is placed in one arm for blood sampling. The research subject may eat a brunch for approximately 15 minutes (sandwich, juice, fried egg and sausage; 550-600kcal) and the p-glucose (mM) is checked at 120 min.
The glucemia after the test meal will be compared in high-carbohydrate diet and high-fad diet (paired samples).
On day 12 of the respective diet
Secondary Enteroscopy: ketogenic activity in the small intestine The biopsy material is fixed deep-frozen for later analyses.The ketonic activity is represented by the activity the ketogenic enzyme mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase (HMGCS2) in the tissue.
Immunofluorescence of antibodies (giving the geography in the duodenal/jejunal mucosa) and western blotting (semi-assessment compared to a steadily-expressed factor in the mucosa, glyceraldehyde 3-phosphate dehydrogenase (GAPDH). The HMGCS2 will be given as ratio to GAPDH. The western blots in the high-carbohydrate diet will be compared to high-fad diet in each individual (paired samples).
On day 14 of the respective diet
Secondary Enteroscopy: mucosal glucose-transport capacity A part of the biopsy-material is kept a short time (<2h) in oxygenated preservation medium. The biopsies are then mounted in Ussing chambers for in-vitro functional studies. Activity of the sodium-glucose linked transporter 1 (SGLT1) is measured as the electrogenic response of 10 mM D-glucose, Iep (µA/mm2), given to the luminal compartment of the Ussing chamber. The net change is the % change of Iep from baseline in the glucose-free condition, to Iep after the addition of glucose to a concentration of 10%. The net change after the high-carbohydrate diet will be compared to the one after high-fat diet in each individual (paired samples). On day 14 of the respective diet
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