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Completed

NCT Number: NCT01387165

Epidemiologic Survey to Describe the Current Medical Practice of General Practitioners Treating Subjects With Type 2 Diabetes Mellitus in Latina

The DEAL (Diabetes En America Latina) study was a multicenter, cross-sectional, epidemiological, questionnaire based study carried out between October 2004 and October 2005 in 9 Latin American countries.

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Key information

About this study

The DEAL (Diabetes En America Latina) study was a multicenter, cross-sectional, epidemiological, questionnaire based study carried out between October 2004 and October 2005 in 9 Latin American countries. General practitioners (GP) from private settings were selected for participation in the study if they were in full time active clinical practice (three or more days per week and treating at least 100 patients per week), had been practicing for at least two years and were seeing at least five type 2 diabetes mellitus (T2DM) patients per week. Over a period of two weeks after receipt of study questionnaires, GPs were required to review the charts of the first 10 (+/- 2) consecutive diabetic patients to visit the clinic and to provide information about their treatment in accordance with the supplied questionnaire.

Patients were eligible for inclusion in the study if they were males or females aged 18-75 with Type II Diabetes Mellitus - T2DM - (defined by the criteria of the American Diabetes Association (12)), were receiving an oral hypoglycemic agent (OHA) or insulin and had given written informed consent, where required. Measurement of glycosylated hemoglobin (HbA1c) performed at the diagnosis and within the previous three months was collected; if the measure was not available for the period, the sponsor supported the laboratory test when necessary, according to the physician's judgment of the patient's need.

Demographic data were collected including information regarding the patient's lifestyle. The most recent fasting blood glucose, lipid level and blood pressure measurements were recorded along with the existence of diabetes related complications such as dyslipidemia, hypertension, macrovascular diseases, eye disorders, kidney disorders, erectile dysfunction and diabetic neuropathy. Antidiabetic medication and/or insulin therapy and therapy for prevention of macrovascular events were also recorded. Information was collected on visits to specialists, challenges to managing the patient's T2DM and on future plans for management. No explanations or clarifications related to the questions were provided and the physicians answered them based on their own understanding. Instructions on how to answer the questionnaire were provided to maximize the validation of the questionnaires.

Descriptive statistical analysis was performed on all variables. Multivariate logistic regression analyses were performed to test the possibility of association between the outcome measures and duration of disease. The independent variables were age, gender, BMI (body-mass index) category, current prescription, drug insurance coverage, glycemic management, lifestyle, number of co-morbidities and compliance to recommendations/therapy. All statistical analyses were conducted using SAS software. A p value <0.05 was considered statistically significant.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Males and females 18-75 years of age, inclusive,
  • Males and females with T2DM, as defined by the criteria of the American Diabetes Association (2003),
  • Males and females under oral anti-diabetics (OAD) or insulin treatment for diabetes and
  • Males and females that have given written informed consent.

Treatment and study plan

treatment

Drug

were receiving an oral hypoglycemic agent (OHA) or insulin

Primary outcomes

  1. The achievement of the planned completed number of questionnaires.

    Time frame: up to 1 year

Secondary outcomes

  1. Changes in glycemic parameters in accordance with the historical information provided by the GPs and her/his judgement of control based on that information.

    Time frame: up to 1 year

  2. Proportion of subjects who respond to any given treatment applied through the level of HbA1c responders (defined as subjects who have achieved HbA1c <7%)

    Time frame: up to 1 year

  3. Assessment of total cholesterol

    Time frame: up to 1 year

  4. Assessment of free fatty acids

    Time frame: up to 1 year

  5. Assessment of high-density lipoprotein

    Time frame: up to 1 year

  6. Assessment low-density lipoprotein

    Time frame: up to 1 year

  7. Assessment of triglycerides

    Time frame: up to 1 year

  8. Assessment of LDL relative flotation

    Time frame: up to 1 year

  9. Assessment of total cholesterol/HDL ratio

    Time frame: up to 1 year

  10. Assessment of LDL/HDL ratio

    Time frame: up to 1 year

  11. Assessment of fasting blood glucose

    Time frame: up to 1 year

Sponsors and collaborators

Lead sponsor

GlaxoSmithKline

Industry

Registry information

Official study title

A Multi-center, Epidemiologic Survey to Describe the Current Medical Practice of General Practitioners Treating Subjects With Type 2 Diabetes Mellitus in Latin America

Acronym: DEAL

Important dates

Study start
2004
Primary completion
2005
Study completion
2005
First posted
Jul 4, 2011
Registry last updated
Jun 8, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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