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Diabetes Mellitus, Type 2 clinical trials

View clinical trials related to Diabetes Mellitus, Type 2.

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NCT ID: NCT02118714 Completed - Diabetes Clinical Trials

Atrasentan Spermatogenesis and Testicular Function

Start date: April 6, 2015
Phase: Phase 2
Study type: Interventional

This study is being conducted to evaluate the effects of Atrasentan on sperm production and testicular function in male subjects with Type 1 or 2 Diabetes and Nephropathy. This study included 2 periods: a Treatment Period (up to 26 weeks) followed by an Observational Period (up to an additional 52 weeks).

NCT ID: NCT02117622 Completed - Clinical trials for Diabetes Mellitus, Type 2

A Non-interventional, Post Marketing Surveillance (PMS) Study of Tresiba® (Insulin Degludec) to Evaluate Long Term Safety and Efficacy in Patients With Diabetes Mellitus in Routine Clinical Practice in India

Start date: July 24, 2015
Phase: N/A
Study type: Observational

This study is conducted in Asia. The aim of the study is to evaluate long term safety and efficacy of Tresiba® (insulin degludec) in patients with diabetes mellitus in routine clinical practice in India.

NCT ID: NCT02117154 Completed - Clinical trials for Diabetes Mellitus, Type 2

Relationship Between HbA1c, Fasting Plasma Glucose, Post-prandial Glucose and Other Measures of Glycemic Control

Start date: June 2013
Phase: N/A
Study type: Observational

This study aims to evaluate relative contributions of fasting plasma glucose and postprandial glucose at various HbA1c levels using 6-day CGM. Evaluation of the relationship between HbA1c, CGM, serum fructosamine and eAG, will also be looked into. HYPOTHESES: 1. Fasting hyperglycaemia is the main contributor in Malaysian T2DM patients with poor glycaemic control (high HbA1c), postprandial hyperglycaemia plays a more important role with lower HbA1c levels. 2. There is good correlation between HbA1c, CGM, serum fructosamine and eAG in Malaysian patients.

NCT ID: NCT02115711 Completed - Hypertension Clinical Trials

Study of a Community Based Approach to Control Cardiovascular Risk Factors in India

SEHAT
Start date: April 2014
Phase: N/A
Study type: Interventional

The study is a 2 year community based cluster randomized controlled trial to assess the role that a community health worker led intervention, in concert with physician education, can play in controlling the principal cardiovascular risk factors, i.e. hypertension, tobacco use, diabetes mellitus, physical inactivity and an unhealthy diet. Participants will include around 3600 adults, 35-70 years of age, from the urban community in the town of Dalkhola, Uttar Dinajpur district, West Bengal, India. The hypothesis of the study is that a community health worker based approach can result in increased control of Hypertension, Diabetes and Smoking.

NCT ID: NCT02115412 Completed - Diabetes Mellitus Clinical Trials

Validation of Medication Non-adherence Model (UK)

Start date: July 2014
Phase:
Study type: Observational

Research has shown that nearly 50% of patients with chronic conditions around the globe do not adhere to their prescribed medicine, leading to enormous cost to the healthcare providers. Non-adherence can be due to various forms and have multiple causes. To address this need, Philips Research has developed Medication Non-adherence model. This tool will help in developing a systemic way of assessing medication non-adherence and providing decision support for targeted intervention to healthcare professionals. The aim of this study is to validate this model with 750 chronically ill patients in UK.

NCT ID: NCT02114814 Completed - Clinical trials for Diabetes Mellitus, Type 2

A Family-Based Diabetes Intervention for Hispanic Adults in an Emerging Community

Start date: June 2012
Phase: N/A
Study type: Interventional

The aim of this study was to compare the efficacy of an intervention and an attention control group in producing changes in diabetes self-management, glycemic control (HbA1c) and health related quality of life in Hispanics with type 2 diabetes. Hypothesis: The experimental group who receive an 8 week intervention program would show significantly greater improvements than an attention control group at 1 and 6 months after the intervention in: behavioral influences of diabetes knowledge, diabetes self-efficacy, and family support, outcomes of self-reported management of diabetes (physical activity, diet, medications, and glucose monitoring), HbA1c levels, and psychological outcomes of health-related quality of life.

NCT ID: NCT02114008 Completed - Obesity Clinical Trials

Residual Gastric Volume in Morbidly Obesa Diabetics. A Comparison of 3 Hour Versus Hour Fasting.

Start date: April 2013
Phase: N/A
Study type: Interventional

To reduce the risk of aspiration for elective procedures, residual gastric volumes (RGV) have traditionally been minimized with overnight fasting. However, prolonged fasting can also have some adverse consequences and has been abandoned for some procedures in several patient populations with the exception of obese and/or diabetic patients. The aim of this study was to assess RGV in morbidly obese diabetic patients after traditional or abbreviated fasting.

NCT ID: NCT02111967 Completed - Clinical trials for Diabetes Mellitus Type 2

Study to Identify Adequate Biomarker to Detect Vitamin B12 Deficiency in Type 2 Diabetic Patients Treated With Metformin

Start date: March 2014
Phase: N/A
Study type: Observational

In this study we compare the vitamin B12 status by measuring serum vitamin B12 and holotranscobalamin in type 2 diabetic patients with and without metformin treatment. Afterwars we investigate which biomarker could be adequate to reflect B12 status in metformin-treated patients. With the help of a questionnaire we assess clinical, nutritional and demographic factors which are associated with vitamin B12 deficiency.

NCT ID: NCT02110979 Completed - Clinical trials for Diabetes Mellitus, Type 2

Validation of a Patient Decision Aid for Type 2 Diabetes

Start date: April 2014
Phase: N/A
Study type: Interventional

The objectives of this study are to compare measurements in knowledge of decision options, support for decision making, uncertainly in decision making, and clarity of values important to decision making among two groups of type 2 diabetes patients, those who receive a Patient Decision Aid and those who receive usual care.

NCT ID: NCT02109978 Completed - Diabetes Clinical Trials

RetroMASTER - Retrospective Cohort MRC ABPI STratification and Extreme Response Mechanism in Diabetes

RetroMASTER
Start date: April 2013
Phase:
Study type: Observational

This study will examine extreme responders to second- and third-line Type 2 Diabetes (T2D) therapy using a retrospective approach and patients with slow or fast diabetes progression.