Effectiveness of Dapagliflozin for Weight Loss
Primary Purpose
PreDiabetes, Obesity, Morbid, Diabetes Mellitus, Type 2
Status
Unknown status
Phase
Phase 2
Locations
Mexico
Study Type
Interventional
Intervention
Dapagliflozin/Metformin
Metformin
Sponsored by
About this trial
This is an interventional treatment trial for PreDiabetes focused on measuring Metformin, Sodium-Glucose Transporter 2 Inhibitors, PreDiabetes, Obesity, Morbid, Diabetes Mellitus, Type 2
Eligibility Criteria
Inclusion Criteria:
- BMI greater than or equal to 40 kg/m^2
- Diagnosis of diabetes or prediabetes according to the criteria of the ADA
- Patients who sign informed consent letter
Exclusion Criteria:
- Use of insulin or sulfonylureas
- Chronic renal failure with glomerular filtration rate <60 ml/min/1.73 m^2
- Use of loop diuretics with no possibility to suspend
- Active genitourinary tract infections determined by symptomatology or urinalysis
- Use of drugs for weight control
- Patients with untreated or uncontrolled hypothyroidism
Sites / Locations
- Hospital de Especialidades Centro Médico Nacional Siglo XXIRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Metformin/Dapagliflozin
Metformin
Arm Description
Metformin 1,700 mg/day and Dapagliflozin 10 mg/day for a year.
Metformin 1,700 mg/day
Outcomes
Primary Outcome Measures
Change in Weight
Change of 10 percent of initial weight
Secondary Outcome Measures
Change in Blood Pressure
Change of 10 percent of initial blood pressure (systolic and diastolic)
Change in Waist Circumference
Change of 10 percent of initial waist circumference
Change in Triglycerides level
Change of 10 percent of initial triglycerides levels
Full Information
NCT ID
NCT03968224
First Posted
May 27, 2019
Last Updated
August 31, 2020
Sponsor
Centro Medico Nacional Siglo XXI IMSS
1. Study Identification
Unique Protocol Identification Number
NCT03968224
Brief Title
Effectiveness of Dapagliflozin for Weight Loss
Official Title
Effectiveness of the Treatment With Dapagliflozin and Metformin Compared to Metformin Monotherapy for Weight Loss on Diabetic and Prediabetic Patients With Obesity Class III
Study Type
Interventional
2. Study Status
Record Verification Date
August 2020
Overall Recruitment Status
Unknown status
Study Start Date
July 7, 2018 (Actual)
Primary Completion Date
July 1, 2021 (Anticipated)
Study Completion Date
July 1, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centro Medico Nacional Siglo XXI IMSS
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
5. Study Description
Brief Summary
Mexico has one of the highest prevalence of obesity, reported on 32.4 percent of people over 20 years old, with a prevalence of obesity class III of 1.8 percent on males and 4.1 percent on females.
According to previous data in our Obesity Clinic the mean age of these patients is 41 years, 46 percent have pre-diabetes or type 2 diabetes mellitus (T2D); 66 percent has hypertension and 33 percent has dyslipidemia. The management of alterations in the glucose metabolism in this unit is made by dietary treatment and with the use of metformin at doses of 1,700 mg/day and/or basal insulin.
Dapagliflozin is a selective SGLT2 inhibitor than has shown a sustained effect on the reduction of glycated hemoglobin at 0.4 to 0.8 percent (initial 7.8 to 8.0 percent). Additionally, due to the induction of glycosuria up to 20 to 85 g/day, it has been calculated that its use induces a caloric deficit at 80 to 340 kcal/day. This has been tested in patients with T2D in which induces a weight loss of 2 to 3 kg and in combination with metformin even a weight loss up to 5.07 kg (-6.21 to 3.93 kg) without regain (at least for 2 years). Furthermore, dapagliflozin decrease systolic blood pressure, increases HDL cholesterol concentrations and decreases triglyceride concentration. The drug product action is independent of the insulin production at pancreas, consequently, it exists a possibility of using the drug product on patients with prediabetes or even on other types of diabetes. Regarding the adverse effects related to its use, it has been described an increase in the risk of genitourinary infections with a low risk for inducing hypoglycemia.
A previous study that included 182 patients with T2D inadequately controlled with metformin assessed the effect of dapagliflozin 10 mg in total weight loss after 24 weeks compared to placebo. It was found a decrease in weight of 2.08 kg (2.8 to 1.31 kg), decrease in waist circumference of 1.52 cm (2.74 to 0.31), decrease in total fat mass assessed with densitometry of 1.48 kg (2.22 to 0.74), decrease of visceral fat mass of 258.4 cm^3 (448.1 to 68.6) and subcutaneous fat of 184.9 cm^3 (359.7 to 10.1). Most of these studies on weight and metabolic control have been performed in patients with obesity class II or I. The aim of this study is to assess if dapagliflozin in combination with metformin is at least 10 percent more effective for weight reduction in comparison with metformin in patients with prediabetes or T2D and obesity grade III.
Detailed Description
Methods:
A convenience sampling will be done for patients diagnosed with diabetes or prediabetes according to the American Diabetes Association (ADA) criteria, who assist to the Obesity Clinic and meet the selection criteria. Data from patients that during the study protocol are called to undergo bariatric surgery procedure will be used until the time of surgery (intention-to-treat analysis). The prevalence of comorbidities at baseline and the type and dose of drugs used for treatment will be recorded. Patients will be randomized by a random numbers system generated with a computational software and will be assigned to a group: metformin (1,700 mg/day) or metformin (1,700 mg/day) and dapagliflozin 10 mg. All patients will receive dietary treatment and follow-up during the study by the Nutrition Service. Once assigned to the corresponding group, patients will receive an identification code that will be retained throughout the study. One of the researchers not directly involved in patient care, will assign tablets needed for daily intake for a month and then the number of tablets required for 3 months in a sealed envelope. A run-in period will be used to assess tolerance to treatments. This period will be for a month. At this time patients may notice an increase of uresis and will be instructed to increase fluid intake. Anthropometric and biochemical variables will be recorded baseline and at 1, 3, 6 and 12 months. The determination of glucagon, ghrelin, adiponectin, resistin, interleukin 6 (IL-6) and interleukin 10 (IL-10) will be held on initial appointment and before surgery (depending on the response of each patient). For the determination of these cytokines and peptides, an ELISA kit (Enzyme Linked Immunosorbent Assay) will be used. Adherence to treatment will be evaluated and will consist in consumption of 90 percent of pills granted. The patient will be required to return the drug blister. The registration of adverse events will take place from the start of treatment and throughout the study. Each event will be evaluated by researchers and classified according to the Common Terminology Criteria for Adverse Events (CTCAE) version 4.03 list. CTCAE considers that an adverse event grade 4 or 5 indicates discontinuation of treatment; grade 3 must be submitted to review by the medical team, and grades 1 or 2 require registration and intervention but not discontinuation of treatment. Adverse events will be recorded in the report sheet. An intention-to-treat analysis will be used if patients require treatment with insulin or sulfonylureas (grade 3 adverse event). They will provide information until the time of its inception. Patients who do not achieve weight loss at one year follow-up, will be discarded to their primary care hospital for continue with dietary recommendations.
Sample Size:
A convenience sample will be performed of patients with obesity class III and prediabetes or diabetes according ADA criteria at Obesity Clinic who meet selection criteria. The sample size was calculated using a mean difference formula with data from Zhang et al. who evaluated weight loss in patients using metformin/dapagliflozin and compared with placebo. Sample size required is 90 patients: 45 patients in metformin group and 45 patients in dapagliflozin/metformin group. Considering a loss of 20 percent of population during study, the final sample size required is 108 patients: 54 patients in metformin and 54 patients in dapagliflozin group.
Statistical analysis Quantitative variables will be presented as means and standard deviation or median with interquartile ranges according to data distribution. Qualitative variables will be presented as frequencies or percentages. For assessing data distribution, a Shapiro-Wilk test will be performed. Association between quantitative variables will be assessed through Repeated measures ANOVA and qualitative variables with McNemar test. Statistical significance will be evaluated with p < 0.05. Statistical analysis will be performed using statistical packages: Statistical Package for the Social Sciences (SPSS) version 17.0.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
PreDiabetes, Obesity, Morbid, Diabetes Mellitus, Type 2
Keywords
Metformin, Sodium-Glucose Transporter 2 Inhibitors, PreDiabetes, Obesity, Morbid, Diabetes Mellitus, Type 2
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Model Description
Randomized single-blind controlled clinical trial
Masking
Participant
Allocation
Randomized
Enrollment
90 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Metformin/Dapagliflozin
Arm Type
Experimental
Arm Description
Metformin 1,700 mg/day and Dapagliflozin 10 mg/day for a year.
Arm Title
Metformin
Arm Type
Active Comparator
Arm Description
Metformin 1,700 mg/day
Intervention Type
Drug
Intervention Name(s)
Dapagliflozin/Metformin
Other Intervention Name(s)
Group 1
Intervention Description
Two tablets of Metformin 850 mg every 12 hours will be provided in combination with Dapagliflozin 10 mg per day. Each participant will receive diet and exercise intervention according to their BMI and current physical condition.
Intervention Type
Drug
Intervention Name(s)
Metformin
Other Intervention Name(s)
Group 2
Intervention Description
Two tablets of Metformin 850 mg every 12 hours will be provided. Each participant will receive diet and exercise intervention according to their BMI and current physical condition.
Primary Outcome Measure Information:
Title
Change in Weight
Description
Change of 10 percent of initial weight
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Change in Blood Pressure
Description
Change of 10 percent of initial blood pressure (systolic and diastolic)
Time Frame
12 months
Title
Change in Waist Circumference
Description
Change of 10 percent of initial waist circumference
Time Frame
12 months
Title
Change in Triglycerides level
Description
Change of 10 percent of initial triglycerides levels
Time Frame
12 months
Other Pre-specified Outcome Measures:
Title
Change in Cytokines Level
Description
Change in interleukin-6, interleukin-10, adiponectin, and resistin, comparing initial versus final levels
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
BMI greater than or equal to 40 kg/m^2
Diagnosis of diabetes or prediabetes according to the criteria of the ADA
Patients who sign informed consent letter
Exclusion Criteria:
Use of insulin or sulfonylureas
Chronic renal failure with glomerular filtration rate <60 ml/min/1.73 m^2
Use of loop diuretics with no possibility to suspend
Active genitourinary tract infections determined by symptomatology or urinalysis
Use of drugs for weight control
Patients with untreated or uncontrolled hypothyroidism
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Aldo Ferreira-Hermosillo, MSc
Phone
+52156276900
Ext
21551
Email
aldo.nagisa@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Moises Mercado, PhD
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital de Especialidades Centro Médico Nacional Siglo XXI
City
Mexico City
ZIP/Postal Code
06720
Country
Mexico
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Aldo Ferreira-Hermosillo, MSc
First Name & Middle Initial & Last Name & Degree
Victoria Mendoza-Zubieta, MSc
First Name & Middle Initial & Last Name & Degree
Claudia Ramírez-Rentería, MSc
First Name & Middle Initial & Last Name & Degree
Mario A Molina-Ayala, MD
First Name & Middle Initial & Last Name & Degree
Etual Espinosa-Cárdenas, MSc
First Name & Middle Initial & Last Name & Degree
Alejandra Albarrán-Sánchez, MD
First Name & Middle Initial & Last Name & Degree
Moisés Mercado, PhD
First Name & Middle Initial & Last Name & Degree
Aldo Ferreira-Hermosillo, MSc
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
Data will be shared upon reasonable request to principal investigator
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