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Type 2 DiabetesNCT02493374

Mitigation of Type 2 Diabetes by Partial Ileal Bypass

An observational study of Type 2 Diabetes, run by University of Minnesota at 1 site in United States.

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record
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Trial summary

This is a study of people with type 2 diabetes and high cholesterol between age 18 and 65. This study is trying to figure out if a partial bypass of the small intestine can reverse type 2 diabetes for people who require cholesterol lowering and who cannot tolerate the statin drugs. Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Type 2 Diabetes
How many people
0 participants
Where
1 siteUnited States
Study dates
May 2016to Jun 2019
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Individuals in need of lipid modification but are intolerant of statin drugs who are referred for a partial ileal bypass (PIB) operation, still the most efficacious means to treat hyperlipidemia. In the subgroup of these patients who also have type 2 diabetes, with a functioning pancreas, we hope to perform a pilot study on the effect of PIB on type 2 diabetes. Study blood tests: - Pre-PIB and at 6 month and 12 months postop fasting blood samples for glucose, hemoglobin A1c, insulin, C-peptide, GLP-1, ghrelin, and glucagon; then after oral glucose meal testing for determination of glucose, GLP-1, and ghrelin at 30, 60, 90, and 120 minutes.

Who may be able to join

  • Hyperlipidemia patients referred for partial ileal bypass, who also have type 2 diabetes.

Who cannot join

  • Preoperative C-peptide indicative of non-functioning islet cells.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • University of Minnesota

    Minneapolis, Minnesota, 55455

Other trials in United States

About this study

Official title: Mitigation of Type 2 Diabetes in Hypercholesterolemic Patients Undergoing a Partial Ileal Bypass

This is a study of people with type 2 diabetes and high cholesterol between age 18 and 65. This study is trying to figure out if a partial bypass of the small intestine can reverse type 2 diabetes for people who require cholesterol lowering and who cannot tolerate the statin drugs.

Read the detailed description

The partial ileal bypass (PIB) operation is a standard procedure used in the management of hyperlipidmia since 1963. POSCH was the intervention modality in the National Institutes of Health, National Heart Lung and Blood Institute-funded Program on the Surgical Control of the Hyperlipidemias (POSCH) trial. The POSCH study was a secondary trial in patients with a documented prior myocardial infarction. The trial compared the post-dietary lipid therapy changes in 421 PIB-intervention patients to 417 controls, with a lowering of total plasma cholesterol of 24% (P<0.0001), a lowering of low density lipoprotein (LDL)-cholesterol of 38% (P<0.0001), and an elevation of high density lipoprotein (HDL)-cholesterol of 4% (P=0.02). These lipid changes were associated with a 35% (P<0.001) reduction in the intervention group of death due to coronary heart disease and confirmed recurrent myocardial infarction, as well as a 27% (P<0.038) reduction in peripheral vascular disease, and a 54% (P<0.005) diminution in the occurrence of coronary artery surgery or angioplasty. Concurrently with the clinical study, POSCH assessed sequential coronary arteriograms at 0, 3, 5, 7, and 10 years, which showed less disease progression in the surgery group, and even statistically significant plaque regression in the PIB cohort. POSCH PIB patients exhibited a statistically significant increase in life expectancy; this finding persisted at a 25-year follow-up assessment.

In the field of metabolic/bariatric surgery, resolution of type 2 diabetes by gastrointestinal tract manipulations was clearly demonstrated by 1998. In three meta-analyses, the procedures that involved shortening of the ileum (biliopancreatic diversion and duodenal switch) were responsible for the highest percentage of type 2 diabetes resolution. Recently under evaluation are standard metabolic/bariatric and experimental metabolic operations that will engender type 2 diabetes resolution with minimal or no weight loss in non-obese diabetic patients.

The gut-diabetes relationship has often been attributed to an increased elaboration of the hormones glucagon-like peptide-1 (GLP-1) and peptide YY (PYY), both secreted by the L-cells of the intestinal mucosa. These hormones seem to work in concert, either eliciting the same metabolic response or augmenting the actions of the other. With respect to pancreatic endocrine function, GLP-1 and PYY contribute to the incretin effect, counteract the insulin depression action of gastrin stimulating peptide and gastrin-releasing peptide, and stimulate glucose-dependent insulin secretion, preinsulin gene expression, beta-cell proliferation, and antiapoptopic pathways. It has been shown that GLP-1 secretion is reduced in patients with type 2 diabetes. In a recent study of the effects of direct human terminal ileum and cecal contact with a food hydrolysate, significant plasma GLP-1 and PYY elevations were demonstrated, confirming the ability of the cecum, as well as the ileum, to secrete GLP-1 and PYY on stimulation. In the Goto-Kakizaki rat with naturally occurring type 2 diabetes, ileal bypass or excision did not lower GLP-1 production, but interestingly increased it five- to six-fold.

These complementary studies gave rise to the hypothesis that: the PIB operation, in addition to its action on cholesterol metabolism, may aslo prevent and resolve type 2 diabetes.

In our laboratory at the University of Minnesota, the investigators have clearly established the mechanism for the reduction of total cholesterol and LDL-cholesterol by PIB: interference with the cholesterol and bile acid enterohepatic cycles, markedly decreased absorption and reabsorption of cholesterol and bile acids, increased excretion of cholesterol and bile acids, increased turnover of cholesterol to generate bile acids and replenish the cholesterol pool, and the insufficient ability of the body (even in familial hypercholesterolemics) to maintain the miscible (plasma and liver) and less-freely miscible (tissues, including the arteries) body pools, and, thereby, a depletion of the cholesterol content of atherosclerotic plaques. the investigators have now (see above) added to that knowledge that the elimination of the terminal ileum from the intestinal pathway will increase circulating GLP-1 levels, with this incretin probably emanating from the cecum.

The investigators have now completed and submitted for publication our study on the incidence of type 2 diabetes in the POSCH program 25 plus years after formal trial closure (IRB Code Number: 1408M53283). The title of our paper is "Partial Ileal Bypass Affords Protection from Onset of Type 2 Diabetes". Of the 66 control patient responders in POSCH, 17 contracted type 2 diabetes (25.8%); of 80 PIB responders, 8 contracted type 2 diabetes (10%). The difference between groups was significant (P=0.015 by Fisher Exact Test) with an odds ratio of 0.320 for the PIB group and an over two-fold (2.6) increase in the incidence of type 2 diabetes in the controls. Including borderline type 2 diabetes (prediabetic) patients, these values were 22 of 66 controls (33.3%) and 10 of 80 PIB patients (12.5%), with an odds ratio of 0.286 and a P<0.004, and again an over two-fold (2.7) increase in the incidence of type 2 diabetes in the control patients. Therefore, PIB appeared to afford protection from the onset of type 2 diabetes for over 30 years.

Conditions
Type 2 Diabetes
Medical subject headings
Diabetes Mellitus, Type 2

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Mitigation of Type 2 Diabetes

    Blood draws only

    Measured: 3 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Jul 2015 (estimated)
  2. Study startMay 2016
  3. Primary completionJun 2018 (estimated)
  4. Study completionJun 2019 (estimated)

Why it stopped: Lack of funding

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
0 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02493374
Sponsor's protocol ID
1504M69662
Status last verified
Apr 2019
First submitted
6 Jul 2015
Last updated
25 Apr 2019
Results posted
No
Data monitoring committee
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Type 2 Diabetes, run by University of Minnesota at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: withdrawn, as of the sponsor's last update on 25 Apr 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was withdrawn before enrolling participants, so there are no results.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Mitigation of Type 2 Diabetes (time frame: 3 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Apr 2019.

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