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日本におけるSGLT2阻害薬と腎性貧血:RWD

基本情報

NCT ID
NCT07063316
ステータス
実施中(募集終了)
試験のフェーズ
-
試験タイプ
観察
目標被験者数
15,000
治験依頼者名
Boehringer Ingelheim

概要

The objectives of the study are: 1. To compare the risk and timing of anemia onset between Sodium-Glucose Co-Transporter-2 (SGLT2) inhibitor users and non-users in patients with chronic kidney disease (CKD) from the index date to first event occurrence or the end date of each individual's follow-up. 2. To compare the following outcomes from the index date to 731 days (24 months) or the end date of each individual's follow-up: A) Longitudinal changes in laboratory values between SGLT2 inhibitor users and non-users in patients with CKD. B) Prescription patterns and treatment regimens for anemia between SGLT2 inhibitor users and non-users in patients with CKD, including analysis of medication types, dosing strategies, and duration of treatments. C) Anemia-related healthcare costs between SGLT2 inhibitor users and non-users.

対象疾患

Chronic Kidney Disease

介入

SGLT2 inhibitor(DRUG)

実施施設 (1)

日本製鉄株式会社 東日本製鉄所 君津診療所

Tokyo, Japan