Real-world Study of CHina Ozempic cLinicAl pRactice in Patients With Type 2 Diabetes (SCHOLAR)

NCT ID: NCT06351748

Last Updated: 2025-04-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

34238 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-01-02

Study Completion Date

2024-03-29

Brief Summary

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This study is to describe the real-world use and impact of semaglutide once-weekly (OW) among participants with type 2 diabetes mellitus (T2DM) in China. Participants diagnosed with T2DM who initiated semaglutide OW for the first time between 1 Jan 2022 (the date when semaglutide OW was listed in the National Reimbursement Drug List \[NRDL\] in China\] and 28 Feb 2023 (9 months prior to the data extraction cut-off date of 30 Nov 2023) will be included in this study. The study period will be 36 months prior to the first date of participants identification period.

Detailed Description

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Conditions

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Diabetes Mellitus, Type 2

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Participants with T2DM

Participants diagnosed with T2DM who initiated semaglutide OW for the first time between 1 Jan 2022 (the date when semaglutide OW was listed in the National Reimbursement Drug List \[NRDL\] in China) and 28 Feb 2023 (9 months prior to the data extraction cut-off date of 30 Nov 2023.

Semaglutide

Intervention Type DRUG

Participants received semaglutide OW according to local label and to routine clinical practice at the discretion of the treating physician.

Interventions

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Semaglutide

Participants received semaglutide OW according to local label and to routine clinical practice at the discretion of the treating physician.

Intervention Type DRUG

Other Intervention Names

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Ozempic

Eligibility Criteria

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Inclusion Criteria

* 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

Exclusion Criteria

* 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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Novo Nordisk A/S

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Clinical Transparency (dept. 2834)

Role: STUDY_DIRECTOR

Novo Nordisk A/S

Locations

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Tianjin Medical University Chu Hsien-I Memorial Hospital

Tianjin, , China

Site Status

Countries

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China

Other Identifiers

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U1111-1296-3151

Identifier Type: OTHER

Identifier Source: secondary_id

NN9535-7877

Identifier Type: -

Identifier Source: org_study_id

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