- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01694446
Regulation of Intestinal and Hepatic Lipoprotein Production by Glucose and Fructose (glucose)
March 6, 2015 updated by: University Health Network, Toronto
Increased postprandial plasma triglycerides are associated with increased cardiovascular risk.
Chronic consumption of carbohydrates is associated with increased levels of triglycerides.
Very few studies have assessed the effect of acute consumption of carbohydrates on plasma triglycerides and lipoprotein production and clearance.
The present study aims to assess the effects of acute administration of glucose and fructose on hepatic and intestinal lipoprotein production.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Each subject will be studied twice 4-6 weeks apart in random order in this single blinded study.
A nasoduodenal tube will be sited under fluoroscopic guidance the day prior to the study.In study A they will receive intraduodenal intralipid (20% at 60 ml/hour) alongside 60 ml/hour of 20% dextrose or fructose for 15 hours starting at 4am.
In study B they will receive 60 ml/hour of intraduodenal intralipid with 60ml/hour of normal saline for 15 hours from 4am.
A pancreatic clamp (octreotide with replacement glucose, insulin, glucagon and growth hormone) will be started at 7am.
From 9am an iv bolus of deuterated-glycerol (d5-glycerol) along with a regular infusion of deuterated leucine (L-[5,5,5-2H3].
Regular blood samples will be drawn to assess lipoprotein kinetics.
Study Type
Interventional
Enrollment (Actual)
14
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ontario
-
Toronto, Ontario, Canada, M5G 2C4
- Toronto General Hopital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
14 years to 56 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Men and women, aged 18 to 60 years
- Body mass index 20 kg/m2 to 27 kg/m2
- Hemoglobin above 130g/L.
- Normal glucose tolerance in response to a 75g, 2-hr OGTT
Exclusion Criteria:
- Subject has a history of hepatitis/hepatic disease that has been active within the previous two years.
- Any significant active (over the past 12 months) disease of the gastrointestinal, pulmonary, neurological, renal (Cr > 1.5 mg/dL), genitourinary, hematological systems, or has severe uncontrolled treated or untreated hypertension (sitting diastolic BP > 100 or systolic > 180) or proliferative retinopathy
- History of diabetes or OGTT indicative of diabetes or impaired glucose tolerance.
- Any history of a MI or clinically significant, active, cardiovascular history including a history of arrhythmia's or conduction delays on ECG, unstable angina, or decompensated heart failure.
- Any laboratory values: AST > 2x ULN; ALT > 2x ULN TSH > 6 mU/l
- Current addiction to alcohol or substances of abuse as determined by the investigator.
- Mental incapacity, unwillingness or language barrier precluding adequate understanding or cooperation
- Taking any prescription or non-prescription medications at the time of the study
- Having donated blood three months prior to and three months post study procedures
A pregnancy test will be performed 1 to 3 days prior to each study in all female subjects. Those who test positive for pregnancy will be excluded.
-
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intraduodenal glucose or fructose
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Assessment of intestinal and hepatic lipoprotein production
Time Frame: 10 hours
|
10 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 2011
Primary Completion (Actual)
January 1, 2013
Study Completion (Actual)
January 1, 2013
Study Registration Dates
First Submitted
September 24, 2012
First Submitted That Met QC Criteria
September 26, 2012
First Posted (Estimate)
September 27, 2012
Study Record Updates
Last Update Posted (Estimate)
March 10, 2015
Last Update Submitted That Met QC Criteria
March 6, 2015
Last Verified
March 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Glucose 090428B
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Hyperlipidemia
-
CSPC Ouyi Pharmaceutical Co., Ltd.Not yet recruitingPrimary Hyperlipidemia
-
Gan & Lee Pharmaceuticals.RecruitingPrimary HyperlipidemiaChina
-
Drug Commission of the German Medical AssociationMadaus AGTerminatedHypercholesterolemia | Combined Hyperlipidemia
-
Misr University for Science and TechnologyActive, not recruiting
-
DongKoo Bio & PharmaUnknownHyperlipidemia, HypertriglyceridemiaKorea, Republic of
-
Chengdu Diao Jiuhong Pharmaceutical FactoryRecruiting
-
Washington University School of MedicineRecruitingHypercholesterolemia and HyperlipidemiaUnited States
-
Jiangsu HengRui Medicine Co., Ltd.Active, not recruitingHypercholesterolemia and HyperlipidemiaChina
-
Jiangsu HengRui Medicine Co., Ltd.CompletedHypercholesterolemia and HyperlipidemiaChina
-
Dr. Md. Alimur RezaRecruitingHyperlipidemia (E.G., Hypercholesterolemia)Bangladesh
Clinical Trials on Intraduodenal glucose or fructose
-
Rockefeller UniversityThe Rogosin InstituteCompletedCardiovascular Disease | Diabetes | Elevated TriglyceridesUnited States
-
The Rogosin InstituteWeill Medical College of Cornell UniversityCompletedCardiovascular Disease | Diabetes | Dyslipidemia | Elevated TriglyceridesUnited States
-
The Rogosin InstituteUniversity of Missouri-Columbia; Weill Medical College of Cornell UniversityTerminatedAdolescent ObesityUnited States
-
Oregon Health and Science UniversityCompletedObesityUnited States
-
University of LausanneCentre Hospitalier Universitaire VaudoisCompletedNormal Physiology on Healthy SubjectsSwitzerland
-
NestléCompletedHealthyNew Zealand
-
Pennington Biomedical Research CenterUSDA Beltsville Human Nutrition Research CenterCompletedBody Weight ChangesUnited States
-
University Hospital, Basel, SwitzerlandCompletedExploratory BehaviorSwitzerland