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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: NCT01060605 Completed - Clinical trials for Diabetes Mellitus, Type 1

Pre Transplant Rapamycin Treatment in Islet Transplantation Alone

ITA-Rp
Start date: October 2001
Phase: Phase 3
Study type: Interventional

Numerous changes to the original Edmonton protocol have been proposed in the attempt of improving the still unsatisfactory long-term function of ITA. Rapamycin may blunt the early inflammatory response to islet transplantation in the liver, thus favoring islet engraftment. Aim of the investigators study was to evaluate the effect of a pre-transplant treatment with rapamycin in patients with type 1 diabetes receiving islet transplant alone and immunosuppression according to the Edmonton protocol.

NCT ID: NCT01060540 Completed - Diabetes Mellitus Clinical Trials

Genetic Testing for Type 2 Diabetes

Start date: August 2010
Phase: N/A
Study type: Interventional

In this 6-month randomized, controlled trial, we examined whether providing participants with genetic test results and counseling regarding their risk for type 2 diabetes would motivate them to improve their health behaviors and lose weight to reduce their diabetes risk. We hypothesized that participants who received conventional diabetes counseling plus genetic test results and counseling would have at least 6 lb greater weight loss at 3 months than participants who received conventional diabetes counseling without genetic test results.

NCT ID: NCT01059825 Completed - Clinical trials for Diabetes Mellitus, Type 2

Study Of Safety And Efficacy Of Ertugliflozin (PF-04971729, MK-8835) In Participants With Type 2 Diabetes (MK-8835-016)

Start date: February 24, 2010
Phase: Phase 2
Study type: Interventional

MK-8835-016 (B1521006) is designed to evaluate the safety and efficacy of an investigational drug, ertugliflozin (MK-8835, PF-04971729) in participants with Type 2 diabetes mellitus. Participants in the study will receive 1 of 6 treatments for 12 weeks including 1 treatment with an approved drug (sitagliptin) for the treatment of Type 2 diabetes mellitus.

NCT ID: NCT01059812 Completed - Clinical trials for Diabetes Mellitus, Type 2

A Pan Asian Trial Comparing Efficacy and Safety of NN5401 and Biphasic Insulin Aspart 30 in Type 2 Diabetes

BOOST™
Start date: February 1, 2010
Phase: Phase 3
Study type: Interventional

This trial is conducted in Asia. The aim of this clinical trial is to compare NN5401 (insulin degludec/insulin aspart (IDegAsp)) with biphasic insulin aspart (BIAsp) 30 in patients with type 2 diabetes not optimally controlled on once or twice daily insulin with or without metformin.

NCT ID: NCT01059799 Completed - Clinical trials for Diabetes Mellitus, Type 2

Comparison of NN1250 Versus Insulin Glargine in Subjects With Type 2 Diabetes

BEGIN™
Start date: February 2010
Phase: Phase 3
Study type: Interventional

This trial is conducted in Asia and Japan. The aim of this trial is to compare insulin degludec (NN1250) with insulin glargine both combined with oral antidiabetic drugs (OADs) in subjects with type 2 diabetes never treated with insulin.

NCT ID: NCT01058772 Completed - Clinical trials for Gestational Diabetes

Gestational Diabetes: Induction Versus Expectant Management of Labour

GINEXMAL
Start date: March 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether, in Gestational Diabetes Mellitus (GDM) pregnancies, induction of labour at 38-39 weeks of pregnancy is superior to expectant management in terms of maternal and neonatal outcomes.

NCT ID: NCT01058733 Completed - Diabetes Mellitus Clinical Trials

Semi-automatic Response System(SARS)in Type 2 Diabetes

SARS
Start date: October 2006
Phase: N/A
Study type: Interventional

Background - Various kinds of interactive online communication systems have been introduced for long-term diabetes management, and their importance in managing patients is increasing. The investigators investigated the amount of physician time needed to maintain such a system, and the investigators developed software to maximise the cost effectiveness. Methods - The investigators conducted a prospective, randomised, controlled trial to investigate the efficacy and safety of a semi-automatic response system (SARS) for online glucose monitoring over a 24-week period of patients with type 2 diabetes. In the SARS group, the "SARS" software filtered the recorded self-monitoring of blood glucose data automatically to reduce the physicians' time, and the physicians managed patients regularly but only manually in the control (manual) group. The investigators measured the time spent by the physicians for online management and compared the HbA1c levels at enrolment and follow-up.

NCT ID: NCT01058577 Completed - Diabetes Mellitus Clinical Trials

Changes in Serum Electrolytes at Different Glucose Concentrations + Impact on a Non-invasive Glucose Monitoring Method

Start date: December 2001
Phase: Phase 1
Study type: Interventional

In healthy subjects: Continuous monitoring of the glucose concentration in the skin by means of a non-invasive glucose sensor during a glucose clamp when systematically changing the blood glucose concentration (e.g. to hyperglycemia). Simultaneous frequent determinations of serum electrolytes.

NCT ID: NCT01055808 Completed - Clinical trials for Diabetes Mellitus, Type 2

Observational Study in Japanese Type 2 Diabetes Patients

INSIGHTS
Start date: January 2010
Phase: N/A
Study type: Observational

This study is designed to address the gap in the literature related to changing treatment regimen or formulation between different types of insulin, and how this change impacts quality of life, adherence, individual patient treatment satisfaction and glycemic control.

NCT ID: NCT01054300 Completed - Clinical trials for Diabetes Mellitus, Type 2

Effects of Once and Twice Daily Dosing Regimen of Ertugliflozin (PF-04971729, MK-8835) In Participants With Type 2 Diabetes (MK-8835-040)

Start date: February 17, 2010
Phase: Phase 1
Study type: Interventional

This is a Phase 1 randomized, double-blind, sponsor open, 4 arm, 2 way cross-over study using 2 cohorts. The objective of the study is to evaluate the pharmacodynamics (PD) effects and the pharmacokinetic (PK) of single day dosing of 2 mg and 4 mg doses of ertugliflozin (Ertu, PF-04971729/MK-8835) each administered once vs twice daily (morning [AM] and evening [PM]) in adults with type 2 diabetes.