The Surgical Treatment of Type 2 Diabetes Mellitus in Non-Morbidly Obese Patients: A Community Hospital Study
NCT ID: NCT01323114
Last Updated: 2011-04-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
66 participants
INTERVENTIONAL
2011-04-30
2014-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Medical Control Group
Control group of patients who will receive conventional medical treatment for type 2 diabetes, along with regular dietary and diabetic education, under the monitoring of the study endocrinologist.
Conventional Medical Treatment
Standard of care medical treatment for type 2 diabetes to include medications and dietary management under the monitoring of the study endocrinologist.
Surgical Treatment Group
Experimental group in which patients will undergo the laparoscopic duodenal bypass procedure along with regular dietary and diabetic education, under the monitoring of the study endocrinologist.
Laparoscopic duodenal exclusion
Laparoscopically-performed Roux-en Y intestinal bypass of the duodenum and proximal jejunum; stomach remains normal size and proximal division performed just distal to pylorus.
Interventions
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Laparoscopic duodenal exclusion
Laparoscopically-performed Roux-en Y intestinal bypass of the duodenum and proximal jejunum; stomach remains normal size and proximal division performed just distal to pylorus.
Conventional Medical Treatment
Standard of care medical treatment for type 2 diabetes to include medications and dietary management under the monitoring of the study endocrinologist.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* fasting blood glucose \> 126 mg/dl
* on hypoglycemic medications for the treatment of type 2 diabetes
* inadequate control of diabetes with glycosylated hemoglobin A1c \> 7.5
* body mass index between 20 and 35
* C-peptide level 1.0 mg/dl or higher
* ability to understand the proposed surgical treatment and its mechanism
* ability to understand the risks and benefits of the proposed surgery
* ability to commit to the study requirements for followup and education
* ability to give properly informed consent for participation
Exclusion Criteria
* previous diagnosis of type 1 diabetes mellitus or mixed diabetes
* pregnancy, within one year postpartum, or currently breastfeeding
* recent (within 1 year) gastric or duodenal ulcer
* use of immunosuppressive medications or known immunosuppressive disorder
* previous gastric, duodenal, or small intestinal surgery
* inflammatory bowel disease
* treatment with anticoagulant or antiplatelet medication other than aspirin 81 mg/day
* end-stage renal disease or on dialysis
* any other serious concomitant medical condition that, in the opinion of the investigator, would compromise the safety of the patient or compromise the patient's ability to participate in the study
20 Years
65 Years
ALL
No
Sponsors
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McKenzie Health System
OTHER
Responsible Party
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McKenzie Health System
Principal Investigators
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Marcus K. Free, M.D.
Role: PRINCIPAL_INVESTIGATOR
McKenzie Health System
Steve Barnett, M.S.
Role: STUDY_DIRECTOR
McKenzie Health System
Locations
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McKenzie Health System
Sandusky, Michigan, United States
Countries
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Central Contacts
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Facility Contacts
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Steve Barnett, M.S.
Role: backup
Other Identifiers
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LDE-199979-1
Identifier Type: -
Identifier Source: org_study_id
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