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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: NCT02824874 Completed - Clinical trials for Diabetes Mellitus, Type II

CKD-396 Drug-drug Interaction Study(A) (CKD-396 DDI(A) P1)

Start date: April 2016
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate a pharmacokinetic drug interaction between lobeglitazone and sitagliptin in healthy male volunteers.

NCT ID: NCT02821117 Completed - Diabetes Mellitus Clinical Trials

FreeStyle Libre Glucose Monitoring System Paediatric Study

SELFY
Start date: June 30, 2016
Phase: N/A
Study type: Interventional

The study is designed to determine glycaemic control achieved using the FreeStyle Libre Flash Glucose Monitoring System (FreeStyle Libre) versus Self-Monitoring Blood Glucose (SMBG) for the self-management of diabetes.

NCT ID: NCT02821052 Completed - Diabetes Clinical Trials

Post-marketing Surveillance (Special Use-results Surveillance) on Long-term Use With Ryzodeg®

Start date: July 1, 2016
Phase:
Study type: Observational

This trial is conducted in Asia. The aim of this Non-interventional study is to investigate the long-term safety and effectiveness of Ryzodeg® (insulin degludec/insulin aspart) in Japanese patients with diabetes mellitus requiring insulin therapy under normal clinical practice conditions.

NCT ID: NCT02819011 Completed - Cancer Clinical Trials

OHI--Randomized Control Trial to Evaluate Efficacy, Acceptability, and Perception of Benefit of an Innovative Custom AFO

Start date: May 2016
Phase: Phase 2
Study type: Interventional

The investigators propose a randomized control trial to evaluate long term effects and effectiveness of Moore Balance Brace (MBB) ankle foot orthoses (AFO) in reducing risk of falling in older adults. Primary Endpoints • Characterize the impact of MBB AFO on balance, gait, risk of falling, frailty status, and adverse events Secondary Endpoints • Characterize the Impact of MBB AFO on spontaneous daily physical activities • Characterize the feasibility of the MBB AFO device on patient adherence, acceptability, user-friendliness, and perception of benefit for daily usage

NCT ID: NCT02817152 Completed - Diabetes Mellitus Clinical Trials

Low-level Laser Therapy in the Treatment of Chronic Periodontitis in Type 2 Diabetics

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

The aim of this study was to investigate the local effect of adjunct low-level laser therapy (LLLT) for the treatment of moderate to severe chronic periodontitis in type 2 diabetic patients.

NCT ID: NCT02814123 Completed - Clinical trials for Diabetes Mellitus, Type 1

Effect of Basal-Bolus Closed-Loop Co-Administration of Insulin and Pramlintide on Improving the Glycemic Control in Type 1 Diabetes

Start date: January 13, 2017
Phase: Phase 2
Study type: Interventional

The closed-loop delivery system is composed of an insulin pump, a continuous glucose sensor and a dosing algorithm that calculates the insulin dose to infuse based on sensor readings. Pramlintide is a drug and an analog of amylin, a hormone that is co-secreted with insulin in healthy individuals, and is deficient in people with type 1 diabetes. Co-injection of pramlintide with insulin at meal times improves glucose control in type 1 diabetes. Literature data suggests that regular insulin may better match the effect of pramlintide compared to rapid insulin in regulating post-prandial glucose levels. The purpose of this study is to compare the effectiveness of 3 strategies to control your day-and-night glucose levels: 1. rapid insulin-alone closed-loop delivery; 2. rapid insulin-plus-pramlintide closed-loop delivery; 3. regular insulin-plus-pramlintide closed-loop delivery. The primary hypotheses are: 1. During closed-loop control, the simultaneous basal-bolus infusion of pramlintide and fast-acting insulin improves glucose control compared to fast-acting insulin-alone infusion. 2. During closed-loop control, the simultaneous basal-bolus infusion of pramlintide and regular insulin improves glucose control compared to fast-acting insulin-alone infusion.

NCT ID: NCT02813759 Completed - Clinical trials for Diabetes Mellitus, Type 2

Sucralose in Subjects With Diabetes Mellitus Insulin Requesting

SDMIR
Start date: July 2015
Phase: N/A
Study type: Interventional

To evaluate the acute effect of a preload of sucralose in presence of carbohydrate (HC) available on the glycemic response, postprandial C peptide and satiety in patients with type 2 diabetes mellitus (DM2) in intensive insulin therapy (IIT).

NCT ID: NCT02813668 Completed - Obesity Clinical Trials

Worksite Lifestyle Program for Reducing Diabetes and Cardiovascular Risk in India

Start date: May 2, 2017
Phase: N/A
Study type: Interventional

This study will test the implementation, effectiveness, cost-effectiveness, and acceptability of a worksite lifestyle improvement program that includes lifestyle education classes led by trained individuals from the worksite and improvements in the worksite environment that will make it easier for employees at risk for diabetes or with unmedicated diabetes to lose weight, exercise more, and eat a healthier diet. A total of 2000 participants across 10 worksites in South, Central, and East India will be involved in this study.

NCT ID: NCT02812303 Completed - Hypertension Clinical Trials

Implementation of a Population Health Chronic Disease Management Program

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

A pilot program was created by the network's primary care leadership team at Massachusetts General Hospital. A population health management program was implemented for chronic disease management. The investigators evaluated quality of care process and outcome measures over the first six months of the program and compared practices assigned a central population health coordinator to those not assigned this support.

NCT ID: NCT02812238 Completed - Clinical trials for Coronary Artery Disease

Study to Evaluate the Effect of Nicotinamide Riboside on Immunity

Start date: June 23, 2016
Phase: N/A
Study type: Interventional

Background: The immune system controls how the body responds to infection or injury. Researchers want to see what effect a dietary supplement called nicotinamide riboside (NR) has on the immune system. A study showed that fasting has a good effect on immune cell health in healthy people. And when immune cells were exposed to NR they had a similar positive response as with fasting. Researchers want to see if healthy people have the same effects from NR and fasting, and if those effects last. Objectives: To see if taking nicotinamide riboside will have the same healthy immune system effects as fasting. To see if these good effects continue even after eating again. Eligibility: Healthy volunteers ages 18 - 39 years Design: Participants will be screened with medical history, physical exam, and blood tests. Women will have a urine pregnancy test. Participants will take 4 pills of either NR or a placebo once a day for 1 week. On day 6, they will not eat or drink anything. On day 7, they will have a study visit to give a blood sample before and after eating a meal at the clinic. They will also give a urine sample. Participants will stop taking the pills for 1 2 weeks. Participants will take either NR or a placebo once a day for 1 week. They will repeat day 6 and day 7 of the first week. Participants will get NR once and placebo once, but will not know which they are taking.