- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04263168
Glycemic Index Variations In the Early Period Following Bariatric Surgery
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Type 2 diabetes mellitus (T2DM) is one of the most prevalent and deadly conditions in the 21st century. T2DM is characterized by obesity and insulin resistance that leads to chronic hyperglycemia, which even with best medical care is often uncontrolled, resulting in life-threatening micro- and macrovascular complications.
The gut microbiota (i.e. the microbial population inhabiting the gut) has been extensively linked to blood glucose levels and was shown to mediate insulin response in various settings, including anti-diabetic pharmacotherapy. Moreover, fecal microbial transplantation (FMT) from lean healthy donors improved insulin resistance in humans suffering from metabolic syndrome. These pre-clinical and clinical evidence suggest that the gut microbiota has a mechanistic role in insulin-resistance.
Bariatric surgeries were originally designed to treat obesity but were also retrospectively found to ameliorate T2DM among other metabolic and non-metabolic disorders. Since obesity is a significant risk factor for T2DM, it is not surprising that surgically-induced weight loss which occurs within several months after surgery also improves insulin sensitivity. However, a substantial share of patients experience an improvement in insulin resistance within days after bariatric surgery, which clinically presents as normal glycemic values despite decreased dosage of anti-diabetic medications in the first post-operative days. This phenomenon of early diabetes remission after surgery precedes any weight-loss, therefore it is weight-independent and it is far from being understood.
Several explanations were suggested to explain early post-bariatric surgery diabetes remission, among which are acute caloric restriction, amplified incretins response, and rapid alterations in bile acids composition; however, none of them accounts for such a drastic improvement in glycemic control within such a short time frame.
Bariatric surgery rapidly alters the gut microbiome in a conserved fashion in both humans and rodents. Although descriptive studies demonstrated a change in microbiome composition within a few months after surgery, most studies didn't analyze microbiome in the first post-operative weeks in which the improvement in diabetes takes place, and data so far remains associative at best. Two independent studies exhibited improved metabolism following FMT from post-bariatric surgery humans and mice donors
into germ-free (microbiota-devoid) mice recipients, however, no mechanism was suggested and both studies used stool samples taken at a very late postoperative period, therefore no conclusions could be made regarding early diabetic remission. Caloric restriction, incretins, bile-acids, and the gut microbiome most probably "co-evolve" following surgery to exert surgery's beneficial metabolic effect with no single factor solely responsible for the entire effect.
Despite being highly effective in ameliorating obesity and obesity-related co-morbidities in the short-term, bariatric surgeries are invasive, risky, and not always successful in the long-term. Bariatric surgeries are thus far from being a perfect solution to obese diabetic patients, but they do serve as an intriguing investigational-model in the context of glucose metabolism. Hopefully, probing the mechanisms behind surgery's metabolic effect will facilitate the development of safer treatments for diabetic patients.
Study Type
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Tel Aviv (Gosh Dan)
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Ramat Gan, Tel Aviv (Gosh Dan), Israel, 52561
- Sheba Medical Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Adult Population (> 18 years old)
- Diabetic Patients (Type 2)
- Bariatric surgery candidates for two types of bariatric surgery, i.e. sleeve gastrectomy and Roux-en-Y gastric bypass
- Laparoscopic Cholecystectomy candidates
Exclusion Criteria:
- Pregnant Women
- < 18 years old
Study Plan
How is the study designed?
Design Details
- Primary Purpose: BASIC_SCIENCE
- Allocation: NON_RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Bariatric Surgery Candidates
All participants will undergo medical and metabolic profiling before surgery at baseline, and during the first two weeks following surgery.
Metabolic profiling will take place during a run-in session in the Sheba medical center, that will include (A) A detailed briefing on study design, goals, samples collection and OGTT, as well as home sample-collecting kit distribution (B) Installation of a continuous glucose monitoring system (CGM, Abbott 'freeStyle Libre').
|
All participants will undergo medical and metabolic profiling before surgery at baseline, and during the first two weeks following surgery.
Metabolic profiling will take place during a run-in session in the Sheba medical center, that will include (A) A detailed briefing on study design, goals, samples collection and OGTT, as well as home sample-collecting kit distribution (B) Installation of a continuous glucose monitoring system (CGM, Abbott 'freeStyle Libre').
|
|
SHAM_COMPARATOR: Laparoscopy Cholecystectomy
All participants will undergo medical and metabolic profiling before surgery at baseline, and during the first two weeks following surgery.
Metabolic profiling will take place during a run-in session in the Sheba medical center, that will include (A) A detailed briefing on study design, goals, samples collection and OGTT, as well as home sample-collecting kit distribution (B) Installation of a continuous glucose monitoring system (CGM, Abbott 'freeStyle Libre').
|
All participants will undergo medical and metabolic profiling before surgery at baseline, and during the first two weeks following surgery.
Metabolic profiling will take place during a run-in session in the Sheba medical center, that will include (A) A detailed briefing on study design, goals, samples collection and OGTT, as well as home sample-collecting kit distribution (B) Installation of a continuous glucose monitoring system (CGM, Abbott 'freeStyle Libre').
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in intestinal microbiota composition prior and following bariatric surgery
Time Frame: two weeks
|
Changes in intestinal microbiota composition following bariatric surgery measured with RNA sequencing
|
two weeks
|
|
Changes in glycemic index prior and following bariatric surgery
Time Frame: two weeks
|
Changes in glycemic index prior and following bariatric surgery measured with continues glucose monitoring system (FreeStyle Libre)
|
two weeks
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (ANTICIPATED)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 6397-19-SMC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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.
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