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Clinical Trials/JPRN-UMIN000009562
JPRN-UMIN000009562Completed未知

Evaluation of the efficacy and safety for switching from premixed insulin to ultra-long acting insulin plus ultra-rapid insulin - Evaluation of the efficacy and safety for ultra-long acting insulin plus ultra-rapid insulin

Department of Endocrinology and Metabolism, Nagoya City West Medical Center0 sites40 target enrollmentStarted: December 17, 2012Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
40

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
20years-old to ot applicable (—)
Sex
All

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1.patients who need insulin therapy newly during this study 2.patients who have allergy for insulin glargine or glulisine 3.patients who had suffered from severe ketosis and diabetic coma or pre-coma 4.patients with serious infection, inflammation, or injury pre- or post- operative state 5.patients who are pregnant, hope to be pregnant, or are in lactation period 6.patients had suffered from drug-induced muscle disorder 7.drug abuser or heavy alcohol drinker

Investigators

Sponsor
Department of Endocrinology and Metabolism, Nagoya City West Medical Center

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