Completed

SCHOLARReal-world Impact of Semaglutide Once-weekly on Type 2 Diabetes Patients in China

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
Study Aim

This study aims to observe the real-world impact of once-weekly Semaglutide treatment on type 2 diabetes patients in China, focusing on changes in Haemoglobin A1c (HbA1c) levels and the proportion of participants achieving HbA1c levels less than 7.0%.

What is being collected

Data Collection

Collected from past medical records and data - Retrospective
Who is being recruted

Diabetes Mellitus+3

+ Diabetes Mellitus, Type 2

+ Endocrine System Diseases

Over 18 Years
+6 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: January 2024
See protocol details

Summary

Principal SponsorNovo Nordisk A/S
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: January 2, 2024

Actual date on which the first participant was enrolled.

This study focuses on understanding the real-life use and effects of a once-weekly medication called semaglutide among individuals with type 2 diabetes in China. The study includes people who have been diagnosed with type 2 diabetes and have started using semaglutide for the first time between January 1, 2022, and February 28, 2023. The goal is to gain insights into how this medication is used in everyday clinical practice and how it impacts patients' health. This research is important as it can provide valuable information on the effectiveness and safety of semaglutide in a real-world setting, potentially improving care for those with type 2 diabetes. During the study, participants will continue with their regular healthcare routine while using semaglutide once a week. The study will measure changes in a substance called Haemoglobin A1c (HbA1c), which gives an idea of average blood sugar levels over the past few months. This will be measured in two units: percentage (%), and millimoles per mol (mmol/mol). Additionally, the study will look at the proportion of participants who achieve an HbA1c level of less than 7.0%. These measurements will help evaluate how well semaglutide helps manage blood sugar levels in people with type 2 diabetes.

Official TitleReal-world Study of CHina Ozempic cLinicAl pRactice in Patients With Type 2 Diabetes (SCHOLAR)
NCT06351748
Principal SponsorNovo Nordisk A/S
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

34238 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Diabetes MellitusDiabetes Mellitus, Type 2Endocrine System DiseasesMetabolic DiseasesNutritional and Metabolic DiseasesGlucose Metabolism Disorders

Criteria

3 inclusion criteria required to participate
Male or female participants aged greater than or equal to (≥) 18 years on index date

Participants with diagnosis of T2DM prior to or on index date

Participants with initiation of semaglutide OW for the first time within the identification period

3 exclusion criteria prevent from participating
Participants with diagnosis of type 1 diabetes prior to or on index date

Participants who were pregnant within 36 months prior to or on index date

Participants who participated in any clinical trials within 36 months prior to or on index date which could be identified from medical records

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Tianjin Medical University Chu Hsien-I Memorial Hospital

Tianjin, ChinaOpen Tianjin Medical University Chu Hsien-I Memorial Hospital in Google Maps
CompletedOne Study Center