Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to Diabetes Type 2 from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 23
- Active, not recruiting: 2
- Completed: 14
- Other: 11
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT05569772 — Semaglutide for the Treatment of Glucose Intolerance in Women With Prior Gestational Diabetes
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Universitaire Ziekenhuizen KU Leuven |
| Enrollment | 252 |
| Study Type | INTERVENTIONAL |
| Conditions | Glucose Intolerance After a Recent History of Gestational Diabetes |
| Interventions | ; |
Gestational diabetes (GDM) is an important contributor to the increasing prevalence of type 2 diabetes (T2DM). Women with glucose intolerance in early postpartum are a particularly high-risk group with about 50% who will develop T2DM within 5 years after the delivery. Moreover, women with a history of GDM progress more rapidly to T2DM compared to women with similarly elevated glucose levels. Ea…
NCT06003153 — GLUCOSE-MGH: Genetic Links Understood Through Challenge With Oral Semaglutide Exposure at MGH
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Massachusetts General Hospital |
| Enrollment | 125 |
| Study Type | INTERVENTIONAL |
| Conditions | Genetic Predisposition; Metabolic Diseases; Type 2 Diabetes |
| Interventions | ; |
The goal of this research study is to evaluate the pathophysiologic mechanisms by which genetic variation impacts response to an FDA-approved medication commonly used to treat type 2 diabetes called oral semaglutide (Rybelsus) and to characterize the physiological response to a mixed meal tolerance test (MMTT) before and after a 14-day treatment with oral semaglutide. The investigators will do …
NCT07689214 — Normast3 for Adults With Diabetic Polyneuropathy
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Roma La Sapienza |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Diabete Type 2 |
| Interventions | ; |
The goal of this clinical trial is to find out if a new supplement called Normast® 3 can help reduce nerve pain and improve nerve function in adults with diabetic polyneuropathy (DPN). DPN is a common complication of diabetes that damages nerves, often causing burning, tingling, or stabbing pain, as well as problems with the autonomic nervous system, which controls things like sweating and hear…
NCT06897475 — A Study of LY3457263 Compared With Placebo in Participants With Type 2 Diabetes on a Stable Dose of Semaglutide or Tirzepatide
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 240 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes |
| Interventions | ; |
The purpose of this study is to measure the change in hemoglobin A1c (HbA1c) with LY3457263 compared with placebo in participants with type 2 diabetes who are not at HbA1c goal when treated with a stable dose of semaglutide or tirzepatide. Participation in the study will last about 9 months.
NCT06943001 — Adapting and Assessing the Feasibility of a Telehealth Diabetes Prevention Program for Hispanic Adolescents
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Baylor College of Medicine |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Obesity and Type 2 Diabetes |
| Interventions |
Hispanic adolescents are disproportionately burdened by type 2 diabetes (T2D). Social determinants of health (SDoH) serve as barriers to behavior change and participation in disease prevention efforts, especially among vulnerable adolescents. Telehealth is a potentially effective approach for delivering disease prevention programs as it addresses some SDoH like transportation, childcare needs, …
NCT06959901 — PATHS-UP Health Behavior Self-monitoring Mobile App for Adolescents
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Baylor College of Medicine |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Obesity and Diabetes Mellitus, Type 2; Diabetes Prevention |
| Interventions |
Hispanic adolescents in the U.S. are disproportionately burdened by type 2 diabetes (T2D) compared to non-Hispanic white youth (0.079% vs. 0.017%) contributing to higher rates of T2D-related vascular complications, cardiovascular disease, and mortality, among this population. Disparities in T2D are driven in part by independent, modifiable risk factors including low levels of physical activity,…
NCT06937203 — A First-In-Human Study of ARO-ALK7 in Adults With Obesity With and Without Type 2 Diabetes Mellitus
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Arrowhead Pharmaceuticals |
| Enrollment | 150 |
| Study Type | INTERVENTIONAL |
| Conditions | Obesity; Diabetes Mellitus, Type 2 |
| Interventions | ; |
This is a Phase 1/2a double-blind dose-escalating study to evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of single and multiple doses of ARO-ALK7 in adult participants with obesity without Type 2 Diabetes Mellitus (T2DM) (Part 1), and the safety, tolerability, and PD of multiple doses of ARO-ALK7 in adult participants with obesity with and without T2DM, eit…
NCT07215559 — A Study of Macupatide (LY3532226) and Eloralintide (LY3841136), Alone or in Combination, in Adults With Obesity or Overweight and With Type 2 Diabetes
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Obesity; Overweight; Diabetes Mellitus, Type 2 |
| Interventions | ; ; |
The purpose of this study is to investigate weight reduction with macupatide and eloralintide, alone or in combination, in adult participants with obesity or overweight and with type 2 diabetes. Participation in the study will last about 48 weeks.
NCT07247084 — A Study of Tirzepatide (LY3298176) Compared With Standard of Care in Adult Participants With Obesity and Without Diabetes (SURMOUNT-REAL UK)
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 3000 |
| Study Type | INTERVENTIONAL |
| Conditions | Obesity |
| Interventions | ; |
The purpose of this study is to evaluate tirzepatide within a real-world setting to assess body weight loss and incidence of type 2 diabetes in adults without diabetes who have obesity and at least one weight-related comorbid condition. Participation in the study will last about 260 weeks.
NCT07307235 — Efficacy and Safety of iGlarLixi Versus Standard of Care in a Real-world Adult China Population With Uncontrolled Type 2 Diabetes on Oral Agents
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Shanghai Zhongshan Hospital |
| Enrollment | 1316 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes |
| Interventions | ; |
This study is a prospective, open-label, multicenter, parallel-group, positive-controlled, and pragmatic randomized clinical trial (pRCT). It will compare the efficacy and safety of iGlarLixi versus standard of care in adult T2DM patients with poor glycemic control, who are using 1 to 3 OADs in a real-world clinical practice setting. A total of 1,316 subjects from approximately 40 research cent…
NCT07282600 — A Study of Eloralintide (LY3841136) in Participants With Obesity or Overweight, and Type 2 Diabetes
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 1035 |
| Study Type | INTERVENTIONAL |
| Conditions | Overweight; Obesity |
| Interventions | ; |
The main purpose of this study is to evaluate the efficacy and safety of eloralintide compared with placebo for body weight reduction in participants with overweight or obesity and type 2 diabetes. Participation in the study will last about 75 weeks.
NCT07399678 — Study of ALV-100 to Assess Safety, Tolerability, and PK/PD in Overweight/Obese Participants With or Without T2D
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Alveus Therapeutics, Inc. |
| Enrollment | 180 |
| Study Type | INTERVENTIONAL |
| Conditions | Overweight or Obese Adults; Overweight or Obese, Type 2 Diabetes |
| Interventions | ; |
A Study of ALV-100 to Assess Safety, Tolerability, and PK/PD in Overweight/Obese Participants with or without Type 2 Diabetes
NCT07321886 — A Study of Eloralintide (LY3841136) in Participants With Obesity, or Overweight Without Type 2 Diabetes
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 1980 |
| Study Type | INTERVENTIONAL |
| Conditions | Obesity; Overweight |
| Interventions | ; |
The purpose of this study is to evaluate the efficacy and safety of eloralintide in adults with obesity or overweight who do not have type 2 diabetes. The study has two phases: a main phase and an extension phase.
Participation in the main phase of the study will last about 75 weeks. Participants with prediabetes will continue in the extension phase for another 2 years.
NCT07392190 — A Study of Eloralintide (LY3841136) in Participants With Persistent Obesity Who Are Treated With a Weekly Incretin
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 900 |
| Study Type | INTERVENTIONAL |
| Conditions | Overweight; Obesity |
| Interventions | ; |
The main purpose of this study is to evaluate the efficacy and safety of eloralintide compared with placebo in participants with persistent obesity or overweight, with or without type 2 diabetes, and on stable incretin background therapy.
Participation in the study will last about 80 weeks.
NCT07400653 — A Study to Learn About the Study Medicine (PF-08653944) in People With Obesity or Overweight and Type 2 Diabetes (T2D)
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Pfizer |
| Enrollment | 999 |
| Study Type | INTERVENTIONAL |
| Conditions | Obesity; Overweight and/or Obesity; Overweight; Diabetes, Type 2; Type 2 Diabetes |
| Interventions | ; |
The purpose of this clinical study is to learn about the safety and effects of the study medicine to help adults with obesity or overweight and type 2 diabetes lose weight. Being overweight or obese means carrying too much body weight. Type 2 diabetes is a condition where there is too much sugar in the blood.
The study medicine is given by a shot under the skin in the belly area. The participa…
NCT06887049 — Achieving Routine Intervention and Screening for Emotional Health
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Chicago |
| Enrollment | 1250 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes Mellitus (T2DM); Diabetes Distress |
| Interventions | ; |
The purpose of this project is to evaluate the effectiveness of diabetes distress screening and intervention on patients with type 2 diabetes mellitus (T2DM).
NCT07606066 — A Study to Identify and Characterize Patients With Type 2 Diabetes Mellitus for Possible Participation in Ongoing or Future Type 2 Diabetes Mellitus Clinical Studies
| Status | Recruiting |
| Phase | N/A |
| Sponsor | AstraZeneca |
| Enrollment | 2150 |
| Study Type | OBSERVATIONAL |
| Conditions | Type 2 Diabetes |
| Interventions |
The purpose of this study is to identify and characterize patients with known Type 2 Diabetes Mellitus (T2DM) for possible participation in ongoing or future T2DM clinical studies, and to characterize trends in key concomitant medication use in this patient population across different geographical regions.
NCT07564414 — A Research Study to Look at How Two Different Doses of CagriSema and One Dose of Semaglutide Help People Living With Obesity With or Without Type 2 Diabetes Lose Weight
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Novo Nordisk A/S |
| Enrollment | 2500 |
| Study Type | INTERVENTIONAL |
| Conditions | Obesity; Type 2 Diabetes |
| Interventions | ; |
This clinical study is testing how the study medicine CagriSema helps people living with obesity, with or without type 2 diabetes (T2D), lose weight. The purpose of the study is to find out how safe and effective CagriSema is for body weight loss in these participants. Participants will receive either CagriSema or semaglutide, and which treatment participants receive is decided by chance. Cagri…
NCT07595549 — A Study to Learn About the Study Medicine Called Berobenatide (PF-08653944) in People With Overweight or Obesity
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Pfizer |
| Enrollment | 954 |
| Study Type | INTERVENTIONAL |
| Conditions | Obesity; Overweight and/or Obesity; Overweight |
| Interventions | ; |
The purpose of this clinical study is to learn about the effects and safety of berobenatide (PF-08653944). This may help people with overweight or obesity lose weight. People in this study may also have type 2 diabetes.
About 950 adults will be in this study. Berobenatide will be compared to a placebo. A placebo does not have any medicine in it but looks just like the medicine being studied. B…
NCT07675161 — MiniMed Fit Payload Wear Pediatric Study
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Medtronic MiniMed, Inc. |
| Enrollment | 100 |
| Study Type | OBSERVATIONAL |
| Conditions | Diabetes (DM); Diabetes (Insulin-requiring, Type 1 or Type 2); Diabetes in Children; Diabetes in Adolescence |
| Interventions |
The purpose of this study is to assess MiniMed Fit Payload adhesive components in different wear locations over a 7-day period to support development of the future commercialized patch pump in participants 7-17 years of age.
NCT07688278 — HbA1c Screening in Dental Care and Primary Care Referral in Patients With Advanced Periodontitis
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Region Skane |
| Enrollment | 600 |
| Study Type | INTERVENTIONAL |
| Conditions | Periodontitis, Adult; Prediabetes / Type 2 Diabetes |
| Interventions | ; |
This study will evaluate whether HbA1c screening can be performed in dental care to detect elevated blood glucose in patients with advanced periodontitis and support referral to primary care.
Periodontitis is a common chronic inflammatory disease affecting the supporting tissues of the teeth. Advanced periodontitis is associated with prediabetes, type 2 diabetes and cardiovascular disease. The…
NCT07690163 — DIabetes GLycemic Assessment in Newly Confirmed Episodes
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Nazarii Kobyliak |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes (T2DM); Obesity Type 2 Diabetes Mellitus; Obesity & Overweight; Insulin Resistance |
| Interventions | ; |
This is a prospective, open-label, randomized controlled trial involving 80 adult patients with newly diagnosed T2DM (diagnosed within the last 3 months) recruited at the Bogomolets National Medical University. Participants may be lifestyle-controlled or receiving stable non-insulin anti-diabetic medications. Participants will be randomized in a 1:1 ratio to either the Real-Time Continuous Gluc…
NCT07592000 — Breakthrough - T1DM and Chronic Kidney Disease
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | University of Chicago |
| Enrollment | 10 |
| Study Type | INTERVENTIONAL |
| Conditions | Diabete Type 1; Chronic Kidney Disease |
| Interventions | ; |
Single arm- subject treated with Tegoprubart and everolimus.
The purpose of this research is to gather information on the safety and effectiveness of investigational regimen containing 2 experimental components:
- An investigational drug called Tegoprubart and
- Human pancreatic islet cells
Both Tegoprubart and human pancreatic islet cells are considered investigational because they are not …
Active, Not Recruiting
NCT06094491 — Virtual Diabetes Group Visits Across Health Systems
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University of Chicago |
| Enrollment | 720 |
| Study Type | INTERVENTIONAL |
| Conditions | T2DM (Type 2 Diabetes Mellitus); Hypertension; Heart Disease Chronic; Stroke; Hyperlipidemias |
| Interventions |
The purpose of this project is to evaluate the effectiveness of a virtual diabetes group visits on patients with type 2 diabetes mellitus (T2DM).
NCT07112872 — A Study to Compare Different Doses of RO7795081 With a Placebo or Semaglutide in People With Type 2 Diabetes
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Hoffmann-La Roche |
| Enrollment | 240 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes Mellitus |
| Interventions | ; ; |
This multicenter, randomized, double-blind, placebo- and open-label active comparator-controlled, parallel-group, dose-range-finding, Phase II study aims to evaluate the efficacy, tolerability, and safety of RO7795081 for glycemic control in adult participants with Type 2 diabetes mellitus (T2D).
Not Yet Recruiting
NCT07684690 — AI-Assisted Antidiabetic Drug Consultation System for Glycemic Control in Type 2 Diabetes Patients Managed by Non-Specialist Physicians
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | National Taiwan University Hospital |
| Enrollment | 400 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes Mellitus (T2DM) |
| Interventions | ; |
This study tests whether an artificial intelligence (AI) tool can help doctors choose better diabetes medicines for their patients. Type 2 diabetes is very common, but there are far more patients than diabetes specialists, so many patients are treated by doctors who are not diabetes specialists. The researchers built an AI consultation system that gives doctors real-time suggestions and predict…
NCT07675187 — HCC Risk and Monitoring in Patients With Type 2 Diabetes
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | National Taiwan University Hospital |
| Enrollment | 2400 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes (T2DM); Hepatocellular Carcinoma (HCC) |
| Interventions |
Liver cancer is a significant malignancy in Taiwan. With the widespread implementation of antiviral therapies, hepatitis B and C-related liver cancer has gradually declined; however, metabolic dysfunction-associated liver cancer continues to increase, particularly among patients with type 2 diabetes mellitus (T2DM) who also present with significant liver fibrosis. Current clinical guidelines la…
NCT07684144 — Extension Trial to Evaluate the Long-term Efficacy, Safety, and Tolerability of Maridebart Cafraglutide (MARITIME-2-EXTENSION)
| Status | Not yet recruiting |
| Phase | Phase 3 |
| Sponsor | Amgen |
| Enrollment | 950 |
| Study Type | INTERVENTIONAL |
| Conditions | Obesity; Overweight; Diabetes Mellitus, Type 2 |
| Interventions | ; |
The primary objective of this trial is to evaluate the long-term efficacy, safety, and tolerability of maridebart cafraglutide in participants with obesity and type 2 diabetes mellitus. Trial 20210182 is extension of trial 20210184 (NCT06858878).
NCT07689877 — Glucose, Understanding, Integrated Digital Health, and Engagement (GUIDE) Study
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Yale University |
| Enrollment | 300 |
| Study Type | INTERVENTIONAL |
| Conditions | Diabetes; Diabetes Type 2 |
| Interventions | ; |
The purpose of this study is to evaluate whether an Integrated Digital Health (IDH) intervention with and without healthcare provider engagement, improves glycemic control and diabetes-related outcomes among adults with Type 2 diabetes. The study will also assess the feasibility of integrating this approach into routine primary care to support personalized, data-informed diabetes management.
NCT06312553 — Remotely Delivered Mindfulness-Based Diabetes Education
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | University of Alabama at Birmingham |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes |
| Interventions | ; |
Diabetes distress is common affecting over one-third of people with type 2 diabetes, negatively impacting self-management and outcomes, and disproportionately affecting low-income individuals. The proposed project will conduct a pilot randomized controlled trial comparing remotely delivered Mindfulness-Based Diabetes Education plus remote patient monitoring of blood glucose to standard Diabetes…
NCT07181304 — Peer Support and Remote Patient Monitoring for Black Adults With Type 2 Diabetes
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | University of Alabama at Birmingham |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes |
| Interventions | ; |
This study will include a type 1 hybrid effectiveness implementation study to evaluate the effectiveness of the PROMOTE (peer support plus remote patient monitoring) program among Black adults with uncontrolled type 2 diabetes recruited from local primary care practices in Jefferson County, Alabama. Additionally, a mixed methods evaluation to characterize the contextual factors relevant to impl…
NCT07376226 — Effects of Whole Fruit on Blood Sugar in People With Type 2 Diabetes
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Harvard School of Public Health (HSPH) |
| Enrollment | 25 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes |
| Interventions |
This study will determine the effects of consuming whole fruit on blood sugar control, liver fat, and cardiovascular health in adults with type 2 diabetes who are not treated with insulin.
NCT07139405 — TriGlytza®-01 Versus Metformin in Overweight and Obese Adults With Type 2 Diabetes and Inadequate Glycaemic Control Despite Metformin Therapy
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | Myopharm Limited |
| Enrollment | 48 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes (T2DM) |
| Interventions | ; ; |
This Phase 2a, randomized, double-blind, active-controlled study will evaluate the safety, tolerability, and preliminary efficacy of TriGlytza®-01 compared with metformin in adults with Type 2 diabetes inadequately controlled despite metformin therapy. Participants will be randomized to one of three treatment groups and treated for 16 weeks. Safety, glycaemic control, body weight, and other met…
Enrolling by Invitation
NCT07688694 — Development of Anti-Diabetic Nutraceuticals From Legume Seed Coats
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | JSS MEDICAL COLLEGE, JSS ACADEMY OF HIGHER EDUCATION AND RESEARCH |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Postprandial Hyperglycemia; Type 2 Diabetes; Metabolic Syndromes |
| Interventions |
This open-label clinical trial aims to evaluate whether daily consumption of soup prepared from boiled water extracts of selected legume seed coats, seasoned with salt and spices, improves glycemic regulation in individuals with metabolic syndrome or type 2 diabetes mellitus (T2DM). The primary question is whether daily intake of this palatable legume-based soup enhances glycemic control. Secon…
Completed Trials
NCT02745613 — Type 2 Diabetes Affect Exercise Induced Improvement in Insulin Sensitivity
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Texas, El Paso |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Insulin Sensitivity/Resistance |
| Interventions |
This study investigates whether: (i) a family history of type 2 diabetes affects exercise induced improvements in insulin sensitivity. (ii) being prediabetic affects exercise induced improvements in glycemic control. (iii) sex differences affect exercise induced improvements in glycemic control.
NCT04255433 — A Study of Tirzepatide (LY3298176) Compared With Dulaglutide on Major Cardiovascular Events in Participants With Type 2 Diabetes
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 13299 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes Mellitus |
| Interventions | ; |
The purpose of the trial is to assess the efficacy and safety of tirzepatide to dulaglutide in participants with type 2 diabetes and increased cardiovascular risk.
NCT04639414 — Combined Active Treatment in Type 2 Diabetes With NASH
| Status | Completed |
| Phase | Phase 4 |
| Sponsor | German Diabetes Center |
| Enrollment | 192 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes; Non-alcoholic Steatohepatitis (NASH); Non-alcoholic Fatty Liver Disease (NAFLD) |
| Interventions | ; ; |
The aim of this multicentre, prospective, placebo-controlled, double-blind, randomized, 3-arm parallel group, interventional study is to assess for the first time the effects of either a combined therapy with the antihyperglycemic drugs semaglutide and empagliflozin or empagliflozin monotherapy compared to placebo as potential treatments for non-alcoholic steatohepatitis (NASH) in patients with…
NCT05715307 — Chinese Endocrinologists Health Education Study
| Status | Completed |
| Phase | N/A |
| Sponsor | Shanghai Jiao Tong University School of Medicine |
| Enrollment | 2017 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes |
| Interventions | ; |
The purpose of this study is to conduct a prospective, multicenter, cluster randomized control study, to evaluate the improvement for T2DM treatment ability in Chinese endocrinologists after 1-week intensive experiential diabetes management training in Ruijin Hospital.
NCT05565534 — Diabetes Care for Breast Cancer Patients
| Status | Completed |
| Phase | N/A |
| Sponsor | Weill Medical College of Cornell University |
| Enrollment | 74 |
| Study Type | INTERVENTIONAL |
| Conditions | Breast Cancer; PreDiabetes; Type 2 Diabetes |
| Interventions |
The goal of this study is to find a new way to make diabetes care better for patients with breast cancer and diabetes who are currently receiving cancer treatment. We will have two groups, the researchers will decide who is in which group. One group will be working with a nurse who is trained in diabetes care while the other does not. This will allow the investigators to see if having a trained…
NCT07669038 — Effects of Online Diabetes Self-management Education on Knowledge Retention, BMI, and HbA1c in Newly Diagnosed Adults With Type 2 Diabetes
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Primorska |
| Enrollment | 123 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes Mellitus (T2DM); Diabetes Self-Management Education |
| Interventions | ; |
Type 2 diabetes requires active self-management from the time of diagnosis, but participation in traditional face-to-face diabetes self-management education is often limited by access-related and personal barriers. Online education may provide a more flexible and accessible way to deliver structured diabetes education, particularly for newly diagnosed adults who need timely support in understan…
NCT05587348 — PROmoting Diabetes Education and Management Through Peer Support and Team Referral
| Status | Completed |
| Phase | N/A |
| Sponsor | University of North Carolina, Chapel Hill |
| Enrollment | 87 |
| Study Type | INTERVENTIONAL |
| Conditions | Diabetes Mellitus, Type 2 |
| Interventions | ; ; |
A 3-step project is proposed. Step 1 will test which BPA time point(s) maximize referral rates to DSMES services in the real world clinic setting (Aim 1). Step 2 will utilize that approach within a pilot study of six sites, comparing the effectiveness of peer support to improve attendance to DSMES services (Aim 2). Step 3 will engage stakeholders in designing a future large scale DSMES services…
NCT06065540 — A Research Study to See How Well CagriSema Compared to Semaglutide, Cagrilintide and Placebo Lowers Blood Sugar and Body Weight in People With Type 2 Diabetes Treated With Metformin With or Without an SGLT2 Inhibitor
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | Novo Nordisk A/S |
| Enrollment | 2734 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes Mellitus |
| Interventions | ; ; |
The study will look at how well CagriSema helps people lower their blood sugar and body weight. CagriSema is a new weekly medicine that combines two medicines called semaglutide and cagrilintide. CagriSema will be compared to the two medicines semaglutide and cagrilintide, when they are taken alone. CagriSema will also be compared to a “dummy” medicine without any active ingredient. The study w…
NCT06144788 — Evaluation of Efficacy and Safety When Administered JP-2266 in Type 2 Diabetes Patients
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Jeil Pharmaceutical Co., Ltd. |
| Enrollment | 161 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes Mellitus |
| Interventions |
A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter, Therapeutic Exploratory Phase 2 Study to Evaluate the Efficacy and Safety of JP-2266 in Patients with Type 2 Diabetes Mellitus
NCT05176210 — Safety, Pharmacokinetics, and Food Effect of PS1 in Subjects
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | Pharmasaga Co. Ltd. |
| Enrollment | 75 |
| Study Type | INTERVENTIONAL |
| Conditions | Type II Diabetes |
| Interventions | ; |
This is a phase I, double-blind, placebo-controlled, randomized, single- and multiple-ascending dose study to evaluate new study intervention, PS1. PS1 is a potential blood glucose control medication, which is developed by Pharmasaga Co. Ltd. planned for treating type II diabetes mellitus (T2DM). This is a first-in-human study to evaluate the safety, tolerability, pharmacokinetics (PK), food ef…
NCT06719076 — IMPACT OF DIABETES HEALTHCARE PROGRAM ON GLYCEMIC CONTROL AND SELF-EFFICACY AMONG TYPE-II DIABETICS IN ISLAMABAD PAKISTAN
| Status | Completed |
| Phase | N/A |
| Sponsor | Health Services Academy, Islamabad, Pakistan |
| Enrollment | 128 |
| Study Type | INTERVENTIONAL |
| Conditions | HbA1c |
| Interventions |
Type 2 Diabetes Mellitus (T2DM) is a significant public health challenge in Pakistan, characterized by a growing prevalence and substantial economic burden. The alarming rise in T2DM cases in Pakistan highlights the need for evidence-based solutions to control the disease. However, there is a notable knowledge gap in the effectiveness of diabetes healthcare program interventions in Pakistan.
T…
NCT07691060 — Asprosin and Total Antioxidant/Oxidant Status in Diabetes and Periodontal Disease
| Status | Completed |
| Phase | N/A |
| Sponsor | Saglik Bilimleri Universitesi |
| Enrollment | 67 |
| Study Type | OBSERVATIONAL |
| Conditions | Periodontal Diseases; Gingival Diseases; Type 2 Diabetes |
The goal of this observational study is to learn about how different periodontal health status affects the levels of asprosin (a hormone) and total oxidant/antioxidant status in the gingival crevicular fluid and blood serum of individuals with Type 2 diabetes.
The main questions it aims to answer are:
Do individuals with Type 2 diabetes and periodontal disease have different levels of asprosi…
NCT07691177 — Bioequivalence Study to Compare Imeglimin HCl 500 mg Film Coated Tablets Versus Twymeeg Tablets 500 mg
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | Humanis Saglık Anonim Sirketi |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes |
| Interventions | ; |
An Open Label, Balanced, Randomized, Single dose, Two treatment, Two sequence, Two period, Two way crossover, Oral Bioequivalence Study of Imeglimin HCl 500 mg Film Coated Tablets of Humanis Sağlık A.Ş., Ç.O.S.B. Karaağaç Mahallesi Fatih Bulvarı No:32 Kapaklı/TEKİRDAĞ and Twymeeg Tablets 500 mg of Sumitomo Pharma Co., Ltd. 2-6-8, Dosho-machi, Chuo-Ward, Osaka City, in Healthy, Adult, Human Part…
NCT07691203 — Bioequivalence Study to Compare Empagliflozin/Linagliptin/Metformin HCl 25 mg/5 mg/1000 mg Extended Release Tablet Versus Trijardy® XR 25 mg/5 mg/1000 mg Extended- Release Tablets
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | Humanis Saglık Anonim Sirketi |
| Enrollment | 36 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes Mellitus (T2DM); Cardiovascular Diseases |
| Interventions | ; |
An open label, randomized, two-period, two treatment, two-sequence, crossover, balanced, single dose oral bioequivalence study to compare Empagliflozin/ Linagliptin/ Metformin HCl 25 mg/5 mg/1000 mg Extended Release Tablet versus Trijardy® XR (Empagliflozin/linagliptin/metformin hydrochloride extended-release tablets 25 mg/5 mg/1000 mg) in healthy subject in fed condition.
Other (Suspended)
NCT01878045 — Mechanisms of Diabetic Kidney Disease in American Indians
| Status | Suspended |
| Phase | N/A |
| Sponsor | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
| Enrollment | 141 |
| Study Type | OBSERVATIONAL |
| Conditions | Nervous System; Diabetic Kidney Disease; Diabetes Mellitus, Type 2 |
Background:
- An ongoing study is looking at American Indians who have kidney problems caused by type 2 diabetes. Kidney disease due to type 2 diabetes is a major problem in American Indians. We previously found that early treatment of kidney disease with losartan was probably beneficial for reducing progression of the disease. Researchers now want to see if these benefits continue to be seen…
Other (Terminated)
NCT04699864 — Evaluation of NeoRetina Artificial Intelligence Algorithm for the Screening of Diabetic Retinopathy at the CHUM
| Status | Terminated |
| Phase | N/A |
| Sponsor | Centre hospitalier de l’Université de Montréal (CHUM) |
| Enrollment | 24 |
| Study Type | INTERVENTIONAL |
| Conditions | Diabetic Retinopathy; Diabetic Macular Edema; Diabetic Maculopathy |
| Interventions | ; ; |
This prospective study aims to validate if NeoRetina, an artificial intelligence algorithm developped by DIAGNOS Inc. and trained to automatically detect the presence of diabetic retinopathy (DR) by the analysis of macula centered eye fundus photographies, can detect this disease and grade its severity.