Investigating significant health trends in growth hormone treatments registry: rationale, aims and design of a nationwide prospective registry (study protocol).
Dirk SchnabelIlonka Kreitschmann-AndermahrChristian J StrasburgerDavid PittrowChristine PauschJoachim Woelflenull nullPublished in: Orphanet journal of rare diseases (2023)
The registry documents children and adults in one joint registry, includes, at present, patients in Germany and allows documentation of patients on all approved somatropin and other growth hormone preparations. It will allow to describe the transition of subjects from adolescence to adulthood (treatment and height), to describe switches between somatotropin preparations, to perform responder analyses, and to analyse differences and similarities of somatropin utilization (by age group, sex, setting, and PRO instrument). INSIGHTS-GHT offers a broad, comprehensive research platform to assess multiple relevant aspects of somatropin treatment and outcomes (including the transition of subjects from adolescence to adulthood), allows the documentation of all GH products including long-acting GH preparations after their introduction, and will evaluate the data independently of funders. Trial registration BfArM Nr. NIS7492, DRKS registry DRKS00027394.
Keyphrases
- growth hormone
- end stage renal disease
- depressive symptoms
- study protocol
- clinical trial
- ejection fraction
- chronic kidney disease
- newly diagnosed
- electronic health record
- prognostic factors
- healthcare
- public health
- young adults
- metabolic syndrome
- body mass index
- high throughput
- machine learning
- mental health
- risk assessment
- health information
- combination therapy
- social media
- smoking cessation
- human health
- single cell