Growth Disorders
Conditions
Brief summary
Assessment of long-term effectiveness of ZOMACTON in treatment of Growth Hormone Deficiency or growth retardation due to Ullrich-Turner Syndrome and assessment of compliance and adherence, optionally with the aid of an electronic app or patient diary.
Interventions
Injection
Sponsors
Study design
Eligibility
Inclusion criteria
* Pediatric patients (\< 18 years) with growth hormone deficiency or growth retardation due to Ullrich-Turner-Syndrome * Patients already receiving or who have been prescribed Zomacton® de novo according to its German label; the decision to prescribe Zomacton® was made independently from participation and prior to enrollment in this study. * Patient and their parents (or legal representatives) who are willing and able to provide signed informed consent for use of their personal data.
Exclusion criteria
* Participation in an interventional clinical study within the last 30 days prior to baseline visit or during the follow-up period
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Linear growth (change in height) | Over the first 12 months (month 0, 3, 6, 9 and 12) | Change in height defined as the change of the standard deviation score of body height vs. baseline |
Countries
Germany