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Study on Risk Factors for Gastrointestinal Adverse Reactions of Semaglutide Injection

Study on Risk Factors for Gastrointestinal Adverse Reactions of Semaglutide Injection

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600116699
Enrollment
Unknown
Registered
2026-01-14
Start date
2026-01-16
Completion date
Unknown
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 2 Diabetes

Interventions

Gastrointestinal Reaction Group:None
Control group:None

Sponsors

Northern Jiangsu People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients with type 2 diabetes initiating semaglutide injection therapy;

Exclusion criteria

Exclusion criteria: 1.Patients who have used other GLP-1RA therapies (e.g., liraglutide, exenatide, lixisenatide, loxenatide, etc.) within the 3 months prior to initiating semaglutide injection treatment. 2.Patients with chronic gastrointestinal diseases presenting with symptoms such as nausea, vomiting, diarrhea, or loss of appetite. 3.Patients unable to provide symptom feedback, such as those with cognitive impairment. 4.Patients with adrenal insufficiency. 5.Non-diabetic individuals or patients with other types of diabetes.

Design outcomes

Primary

MeasureTime frame
The starting dose;Alcohol drinking history;Transaminase;Sex;Glycated Hemoglobin (HbA1c);Age;Smoking history;Concomitant Medications;Serum Creatinine;Infection Status;Gastrointestinal Symptoms;Bilirubin;Body Mass Index (BMI);

Countries

China

Contacts

Public ContactMao Leilei

Northern Jiangsu People's Hospital

418978627@qq.com+86 514 87373418

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026