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NordiNet® International Outcome Study-Observational Prospective Study on Patients Treated With Norditropin®
This observational study is conducted globally. The aim of the study is to investigate the effectiveness and safety of real-life treatment with Norditropin®. The study population will consist of children and adults who are on treatment with Norditropin® in accordance with normal clinical practice.
Age
All ages
Sex
ALL
Healthy Volunteers
No
Novo Nordisk Investigational Site
Prov. de Buenos Aires, Argentina
Novo Nordisk Investigational Site
Brussels, Belgium
Novo Nordisk Investigational Site
Prague, Czechia
Novo Nordisk Investigational Site
Copenhagen S, Denmark
Novo Nordisk Investigational Site
Espoo, Finland
Novo Nordisk Investigational Site
Paris La Défense Cedex, France
Novo Nordisk Investigational Site
Mainz, Germany
Novo Nordisk Investigational Site
Budapest, Hungary
Novo Nordisk Investigational Site
Dublin, Ireland
Novo Nordisk Investigational Site
Kfar Saba, Israel
Start Date
April 1, 2006
Primary Completion Date
December 31, 2016
Completion Date
December 31, 2016
Last Updated
October 12, 2017
21,249
ACTUAL participants
somatropin
DRUG
somatropin
DRUG
Lead Sponsor
Novo Nordisk A/S
NCT06109935
NCT05230550
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT04970654