jRCT1032230486进行中(未招募)不适用
Questionnaire survey on the use of the OneDrawTM automated blood collection and storage device in patients with type 2 diabetes
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 入组人数
- 30
- 主要终点
- -
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18age old over 至 No limit(—)
- 性别
- All
入选标准
- •Patients who meet all of the following criteria will be considered.
- •Age 18 years or older on the date of consent, regardless of gender
- •Outpatients with mild to moderate type 2 diabetes whose condition is stable
- •Patients who are able to adhere to medication adherence and diet and exercise regimen as directed
- •Patients with HbA1c less than 8.0% on the last 2 diabetes examinations prior to obtaining consent
- •Patients who have not changed their diabetes medications since the two previous visits at the time of obtaining consent and have no plans to do so until the end of this study
- •Patients who have received a thorough explanation of their participation in this study, and who have given written consent of their own free will based on sufficient understanding
排除标准
- •Patients who violate the following criteria will be excluded from this study.
- •Patients with type I diabetes mellitus
- •Patients on insulin therapy
- •Patients who may exhibit severe ketosis, diabetic coma or pre-comatose state during study participation
- •Patients with unstable HbA1c levels
- •Patients with restrictions on diet and exercise due to other diseases or complications
- •Patients who are pregnant, lactating, may be pregnant, or are planning to become pregnant
- •Patients with impaired hemostatic function due to bleeding disorder or medication, or with shock or allergy
- •Other patients deemed by the physician to be ineligible for participation
结局指标
主要结局
-
Results of a survey on the use of the OneDra for patients with type 2 diabetes
次要结局
未报告次要终点
研究者
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