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Type 2 Diabetes clinical trials

View clinical trials related to Type 2 Diabetes.

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NCT ID: NCT03329118 Not yet recruiting - Type 2 Diabetes Clinical Trials

Drug-drug Interaction Between Simvastatin and SHR3824

Start date: November 24, 2017
Phase: Phase 1
Study type: Interventional

the purpose of thr study is to investigate the potential interation between multiple oral doses of SHR3824 and single oral dose of Simvastatin in healthy adult volunteers.

NCT ID: NCT03315780 Completed - Type 2 Diabetes Clinical Trials

A Study of the Glucodynamic Effects of Dulaglutide (LY2189265) in Japanese Participants With Type 2 Diabetes

Start date: October 28, 2017
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the glucodynamic effects of dulaglutide in Japanese participants with type 2 diabetes mellitus.

NCT ID: NCT03311724 Completed - Type 2 Diabetes Clinical Trials

A Study of Tirzepatide (LY3298176) in Participants With Type 2 Diabetes

Start date: October 19, 2017
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the efficacy of tirzepatide in participants with type 2 diabetes.

NCT ID: NCT03301792 Active, not recruiting - Type 2 Diabetes Clinical Trials

Group Versus Traditional Prenatal Care for Diabetes

Start date: September 14, 2017
Phase: N/A
Study type: Interventional

The investigators primary objective is to conduct a randomized trial to determine the effect of diabetes group prenatal care on glycemic control and postpartum weight retention in women with type 2 diabetes and gestational diabetes.

NCT ID: NCT03299153 Completed - Type 2 Diabetes Clinical Trials

The Effects of Barberry Juice Consumption in Patients With Type 2 Diabetes

Start date: December 21, 2016
Phase: Phase 4
Study type: Interventional

The aim of this study was to investigate the effect of barberry juice (BJ) as a natural antioxidant, on cardiovascular risk factors in patients with type 2 diabetes (T2DM). In a randomized clinical trial study, 46 T2DM patients, 30-70 years old recruited from "Diabetes Association of Iran-Babul ". Patients were randomly allocated to either the BJ group (n=23) who consumed 200 ml of BJ daily for eight weeks, or the control group (n=23) with no intervention. At the baseline and the end of 8-week intervention, blood pressure and biochemical markers were conducted.

NCT ID: NCT03285750 Completed - Type 2 Diabetes Clinical Trials

Expression of G-protein Coupled Receptor 120 Receptor in Adipose Tissue of German Diabetes Center Cohort Subjects

GPR120
Start date: August 2013
Phase:
Study type: Observational

G-protein coupled receptor 120 (GPR120) is a G-protein-coupled receptor whose endogenous ligands have been identified as long-chain fatty acids. Recently, it has been shown that GPR120 expression in human adipose tissue is higher in obese than in lean individuals. Interestingly, a GPR120 deficient mouse model presents an unfavorable phenotype when fed a high-fat diet with obesity, glucose intolerance and fatty liver, characteristics also found in type 2 diabetes (T2D). Moreover, in obese subjects, a single nucleotide polymorphism (R270H) has been identified that inhibits GPR120 signaling activity. The investigators now want to investigate if GPR120 expression in adipose tissue may be altered in patients with T2D compared to non-diabetic subjects and might contribute to diabetes-associated metabolic changes. Additionally, the investigators want to assess the frequency of the R270H mutant in T2D.

NCT ID: NCT03269058 Completed - Type-2 Diabetes Clinical Trials

Evaluate the Effects of Dapagliflozin in Patients With Type 2 Diabetes

Cinétique DAPA
Start date: December 20, 2017
Phase: Phase 4
Study type: Interventional

This study will make it possible to better understand the mechanisms responsible for the increase in bad cholesterol levels observed in patients with type 2 diabetes treated with Dapagliflozin, an antidiabetic treatment made by Astrazeneca. The information will: - reveal what is not working properly - make it possible to choose the most appropriate treatments against cholesterol to compensate for this impaired functioning This biomedical research will take place at the University Hospitals of DIJON and NANTES. - 28 patients will take part: 20 patients will be given Dapagliflozin and 8 patients will be given the placebo. - The study treatment will be randomised: patients will be given either Dapagliflozin or the placebo. The treatment duration is 6 months. - Moreover, during the inclusion visit and at the end of the study (6 months after the start of treatment), a kinetics study, to follow the production and elimination of cholesterol, will be conducted. This will involve administering amino acids that have been specifically synthesised for this purpose. - Participation in the study will last 6 months and include 4 protocol visits.

NCT ID: NCT03223389 Not yet recruiting - Type 2 Diabetes Clinical Trials

Fat Metabolites and Gut Hormones

Start date: August 7, 2017
Phase: N/A
Study type: Interventional

To investigate the effects of different fat metabolites on gut hormone secretion in gastric bypass operated subjects and BMI-matched controls.

NCT ID: NCT03199261 Completed - Type 2 Diabetes Clinical Trials

A Study of Pharmacokinetic Comparison of Two Recombinant Exendin-4 Formulations in Chinese Healthy Male Subjects

Start date: December 23, 2016
Phase: Phase 1
Study type: Interventional

Evaluation of the pharmacokinetics and safety rE-4 Injection versus rE-4 Freeze-dried Powder in healthy subjects.

NCT ID: NCT03144505 Completed - Type 2 Diabetes Clinical Trials

Comparing Moderate and High-intensity Interval Training Protocols on Biomarkers in Type 2 Diabetes Patients

D2FIT
Start date: February 2014
Phase: N/A
Study type: Interventional

To overcome the lack of knowledge regarding the relative role of different intensities of aerobic training in adults with type 2 (T2D) diabetes, a 12 month randomized controlled trial will be performed to assess and compare the impact of two exercise groups: 1- high intensity interval training (HIIT) with resistance training; 2- moderate continuous training (MCT) with resistance training; and 3- a standard counseling home based control group; on hemoglobin A1c (HbA1c) as the main outcome, and other selected cardiometabolic, body composition and quality of life markers, as secondary outcomes. This investigation aims to increase the current knowledge on HIIT and the related benefits on diabetes control and treatment in a time saving and physiological efficient framework, which will improve the general health and well-being of the diabetes population. A total of 105 participants with T2D will be recruited from the Lisbon area (35 control, 35 HIIT, and 35 MCT). The investigators hypothesize that high-intensity interval training, compared to moderate continuous training, will optimize the physiological adaptations and quality of life in people with type 2 diabetes.