跳至主要内容
临床试验/NCT07621419
NCT07621419招募中不适用

New Formulation of Semaglutide in the Treatment of Type 2 Diabetes in Argentina: a Prospective, Multicenter, Real-world Study

Hospital Italiano de Buenos Aires2 个研究点 分布在 1 个国家目标入组 145 人开始时间: 2025年8月4日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
145
试验地点
2

研究概览

简要总结

The goal of this prospective, multicenter, observational study is to evaluate the real-world effectiveness and safety of oral and subcutaneous semaglutide in adults with type 2 diabetes mellitus in Argentina. The main objective is to assess changes in glycated hemoglobin (HbA1c) from baseline to 3, 6, and 12 months after treatment initiation. Secondary objectives include evaluating changes in body weight, waist circumference, hand-grip strength, treatment satisfaction, medication adherence, treatment route switching, treatment discontinuation, and adverse events.

Participants will receive semaglutide as prescribed by their treating physician as part of routine clinical care. Follow-up assessments will be performed at 3, 6, and 12 months to collect clinical, laboratory, safety, treatment satisfaction, and adherence data. Treatment satisfaction will be assessed using the Diabetes Treatment Satisfaction Questionnaire (DTSQ), and adherence will be assessed using the Simplified Medication Adherence Questionnaire (SMAQ).

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥ 18 years.
  • Clinical diagnosis of type 2 diabetes mellitus.
  • Baseline glycated hemoglobin (HbA1c) >7% and ≤12%.
  • Initiating treatment with semaglutide (oral or subcutaneous) prescribed by the treating physician according to clinical judgment.

排除标准

  • Pregnancy or lactation at the time of enrollment.
  • History of severe hypersensitivity or adverse reactions to glucagon-like peptide-1 (GLP-1) receptor agonists.
  • Contraindications to semaglutide as listed in the product label (e.g., severe gastrointestinal disease, certain endocrine tumors).
  • Any other serious medical condition that, in the investigator's opinion, may interfere with study participation or data interpretation.

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ivan A. Huespe

Head of Research ICU

Hospital Italiano de Buenos Aires

研究点 (2)

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