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French Registry of Children Treated With Norditropin® for Short Stature Associated With Noonan Syndrome

Noonan Syndrome Clinical Trial

Official title:
French Registry of Children Treated With Norditropin® for Short Stature Associated With Noonan Syndrome

Clinical Trial Summary

This is a non-interventional registry of children treated with Norditropin® for short stature due to Noonan Syndrome (NS). This study aims to provide data on long-term growth evolution and safety of Norditropin® as well as Health Related Quality of Life (HRQoL) data. This registry will include the entirety of children treated with Norditropin® for short stature due to NS over the inclusion period. The decision to initiate treatment with commercially available Norditropin® is made by the patient/parents/Legally Acceptable Representative (LAR) and the treating physician before and independently from the decision to include the patient in this study.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05308927
Study type Observational
Source Novo Nordisk A/S
Contact
Status Enrolling by invitation
Phase
Start date March 16, 2022
Completion date March 17, 2028
View Details
See also
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