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Clinical Trial Summary

The main purpose of this study is to evaluate the effect of excipients sodium citrate and treprostinil without insulin on local infusion site pain in participants with type 1 diabetes mellitus (T1DM) on continuous subcutaneous insulin infusion (CSII). The study may last up to 36 days including a screening period and 3 visits.

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT05067270
Study type Interventional
Source Eli Lilly and Company
Contact There may be multiple sites in this clinical trial. 1-877-CTLILL
Phone 1-317-615-4559
Email [email protected]
Status Not yet recruiting
Phase Phase 1
Start date October 22, 2021
Completion date December 15, 2021

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