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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02977039
Other study ID # 2016P000321
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date November 2019
Est. completion date June 2020

Study information

Verified date January 2020
Source Beth Israel Deaconess Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the effect of a nutrient dense plant rich (NDPR) diet compared to a standard USDA diet on glycemic control, inflammation, and cardiovascular risk in individuals with type 2 diabetes and overweight/obesity.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date June 2020
Est. primary completion date January 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

1. Men and women ages 18-75

2. Type 2 diabetes mellitus diagnosed > 6 months prior to screening visit according to American Diabetes Association criteria

3. HBA1c >7.5% but < 10%

4. BMI >25 kg/m2 ; >23 kg/m2 for Asian subjects but < 45 kg/m2

5. Stable weight (variation < 5 kg within 6 months of screening visit)

6. Ability to give informed consent

7. Ability to follow verbal and written instructions in English

Exclusion Criteria:

1. Active cardiac issues: history of myocardial infarction within 3 months of screening visit, unstable angina pectoris, or Class III or Class IV congestive heart failure

2. Persistent uncontrolled hypertension (BP > 160/100 mmHg on or off antihypertensive medication)

3. Active marijuana or intravenous drug use

4. Recent weight loss (> 5 kg within 6 months of the screening visit)

5. Inflammatory or irritable bowel disease (Crohn's Disease, Ulcerative Colitis, or IBS)

6. Celiac disease

7. Malignancy treated with chemotherapy within the past 1 year

8. Depression or psychosis requiring hospitalization within 1 year, or use of major antipsychotic or tranquilizer drugs (i.e. benzodiazepines)

9. Renal insufficiency (creatinine clearance < 30 ml/min)

10. Transaminases > 2x above the normal range

11. Pregnancy within 6 months of the screening visit

12. Lactation

13. History of surgery for the treatment of obesity (gastric banding, gastric bypass, gastric stapling

14. History of alcohol abuse within the past 5 years

15. Vegetarian/Vegan diet

16. Dairy Allergy/Intolerance

17. Anemia, including iron deficient and megaloblastic

18. Vitamin B12 deficiency

19. Leber's disease

Study Design


Related Conditions & MeSH terms


Intervention

Other:
NDPR diet
nutrient rich plant based diert
USDA healthy eating diet
DASH diet

Locations

Country Name City State
United States Beth Israel Deaconess Medical Center Boston Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Beth Israel Deaconess Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Glycemic control A1C and finger stick blood sugar levels change at 1, 3, 6, 9, 12 months
Secondary body weight change at 1, 3, 6, 9, 12 months
Secondary body composition DXA scan change at 1,3,6,9, 12 months
Secondary hepatic steatosis MRspectroscopy baseline, 1, 3, 6, 9, 12 months
Secondary inflammatory markers serum inflammatory markers change at, 1, 3, 6, 9, 12 months
Secondary quality of life validated questionnaired change at, 1, 3, 6, 9, 12 months
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