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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03194009
Other study ID # 102/100/00/16
Secondary ID
Status Recruiting
Phase N/A
First received June 2, 2017
Last updated March 5, 2018
Start date August 10, 2017
Est. completion date December 31, 2022

Study information

Verified date March 2018
Source Instituto Nacional de Salud Publica, Mexico
Contact Luz María Sánchez-Romero, MD, PhD
Phone +52 (55) 54871000
Email luz.sanchez@insp.mx
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The PRuDENTE study proposes to assess if metformin therapy a viable, efficient and cost-effective intervention to decrease the incidence of type 2 diabetes (DMT2) in adult subjects with obesity and pre-diabetes in Mexico City. Half of the individuals recruited will receive as intervention, metformin and lifestyle modification therapy and the other half will receive only lifestyle modification therapy.


Description:

Diabetes in Mexico is considered a national emergency given its high prevalence, incidence, mortality and costs. Mexico has one of the highest prevalence of diabetes; in only 6 years (2000 to 2006) this prevalence increased from 7.5% to 14.4%. In 2015, 151 deaths per 100,000 inhabitants occurred in Mexico due to diabetes complications.

Metformin is a hypoglycemia drug and it´s the first line medication for the treatment of type 2 diabetes.There is currently a significant amount of evidence that metformin administration reduces the progression from pre-diabetes to diabetes and, despite its monotherapy being less effective than lifestyle changes, the good biosafety profile and low cost have made it the drug of choice in a joint treatment.

The PRuDENTE study proposes to perform this intervention in a real environment in the clinics of the first level of care of the Ministry of Health of the Government of Mexico City, in order to provide evidence about the cost-effectiveness of metformin as a public health intervention for the prevention of diabetes.


Recruitment information / eligibility

Status Recruiting
Enrollment 3060
Est. completion date December 31, 2022
Est. primary completion date December 31, 2020
Accepts healthy volunteers No
Gender All
Age group 30 Years to 65 Years
Eligibility Inclusion Criteria:

- Having received primary care in the chosen health center (ideally two or more visits to that clinic in the prior year).

- Subscribers to "Seguro Popular" ( Mexican national health insurance)

- Body mass index >=30 kg / m2

- Results of fasting serum glucose with values for pre-diabetes diagnosis (glucose between 100 and 125 mg / dl)

Optional:

- Family history of DMT2 (1st grade relative).

- Previous diagnosis of hypertension or dyslipidaemia.

- Have received antihypertensive medication and / or for cholesterol / lipids.

- History of gestational diabetes mellitus.

Exclusion Criteria:

- Renal insufficiency (Glomerular Filtration Rate (GFR) <30 ml/min).

- Known hepatic impairment or altered liver enzymes (aspartate aminotransferase (AST) AST or alanine aminotransferase (ALT) three times above normal values)

- Active alcoholism or drug addiction

- Allergies or previous known intolerance to exercise or metformin.

- Current pregnancy.

- Plans to leave the area in the next three years.

- Previous diagnosis of type 2 diabetes mellitus

Study Design


Intervention

Drug:
Metformin
The patient will received metformin 1 tablet of 850mg every 12 hrs besides lifestyle modification recommendations
Behavioral:
Lifestyle intervention
The patient will received recommendations to modify their diet and increase their physical activity every three months towards prevention of diabetes

Locations

Country Name City State
Mexico Centros de Salud. Secretaría de Salud Ciudad de México Mexico City

Sponsors (4)

Lead Sponsor Collaborator
Instituto Nacional de Salud Publica, Mexico Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Ministry of Health, Mexico City, University of California, San Francisco

Country where clinical trial is conducted

Mexico, 

Outcome

Type Measure Description Time frame Safety issue
Primary Diabetes. measured by HbA1c and Fasting blood glucose (FBG) We define type 2 diabetes (T2D) as either FBG 100-125 mg/dl or HbA1c of >= 6.5% 3 years
Primary Lifestyle modifications by decreasing adiposity indicators We will evaluate this by : weight in Kg, height in mts. They also be combined to report BMI/m2, and waist circumference Will be evaluated every 3 months during the 36 month period
Primary Caloric intake From food-frequency questionnaires. Every 3 months during the 36 month period
Primary Physical Activity Expresses ad the average metabolic equivalents (METs)-hours/week Every 3 months during the 36 month period
Secondary Implementation process outcomes at the clinic level. Using a questionnaire Assess the implementation process outcomes at the clinic-, clinician- and patient-levels that will explain the observed effectiveness, and enable future efforts to adapt and disseminate the intervention model across other primary care settings. A questionnaire will be develop to assess the feasibility and limitations for the longterm implementation of this intervention 5 years
Secondary Implementation process outcomes at the clinician level. Using a questionnaire A questionnaire will be develop to assess the limitations of recruitment at the clinic . As well as to evaluate the feasibility of continuing this intervention in outside patients. 5 years
Secondary Implementation process outcomes patient level. Assess via questionnaire Assess the implementation process at the patient-levels using a questionnaire that show data regarding adherence to treatment and lifestyle modifications. 5 years
Secondary Cost-utility of Metformin. Measured using cost per QALYS Analyse the cost-utility of the implementation of this intervention in primary-care health. Using direct and indirect health-care cost data. 5 years
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