Viewing Study NCT00450190



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Last Modification Date: 2024-10-26 @ 9:31 AM
Study NCT ID: NCT00450190
Status: COMPLETED
Last Update Posted: 2018-07-23
First Post: 2007-03-21

Brief Title: Saizen E-Device User Trial
Sponsor: Merck KGaA Darmstadt Germany
Organization: Merck KGaA Darmstadt Germany

Study Overview

Official Title: User Trial on the Use in Common Practice of a New Electronic Auto-injector of Saizen the E-Device Electronic Device in Children Treated by Recombinant Human Growth Hormone Over a Period of 2 Months
Status: COMPLETED
Status Verified Date: 2017-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The aim of the study is to evaluate the E-Device performances and handling on the use in common practice by collecting the impressions of patients nurses and the investigator on the graphic interface the instructions manual the E-Device training and the material itself
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None