Influence of Adherence to Growth Hormone Therapy (GHT) With Norditropin® on Near Final Height in Patients With Growth Hormone Deficiency (GHD) and Born Small for Gestational Age (SGA)
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Norditropin® FlexPro®.
- Who it may be relevant to
- Registry conditions: Growth Hormone Deficiency in Children, Born Small for Gestational Age. Basic parameters: 0 years — 15 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Germany
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
A Non-interventional, Prospective Study in Germany to Investigate the Influence of Adherence to Growth Hormone Therapy (GHT) With Norditropin® on Near Final Height in a Patient Population With Isolated Growth Hormone Deficiency (GHD) and Born Small for Gestational Age (SGA)
Overview
Participants are free to decide if they want to take part in this study or not. The study will be conducted to collect information about the influence of adherence to growth hormone therapy with Norditropin® in children and teenagers in daily practice in Germany. This study will look mainly at the difference in near final height between children and teenagers who adhere to their therapy plan with Norditropin® to non-adherent patients. Participants will get Norditropin® as prescribed to them by their doctor. The study will last as long as the therapy with growth hormone is seen necessary by the participants' doctors and the participants, up to a maximum of 10 years. During the visits at the participants' doctors participants will be asked to fill in a questionnaire.
Interventions
- Drug Norditropin® FlexPro®
Patients will be treated with commercially available Norditropin® FlexPro® according to routine clinical practice at the discretion of the treating physician. The decision to initiate treatment with commercially available Norditropin® FlexPro® has been made by the treating physician and the patient's parents/legal guardian before and independently of the decision to include the patient in this study.
Primary outcome measures
- Near final height (NFH) standard deviation score (SDS) measured in scores [Time frame: At the end of the study (up to 10 years)]
Secondary outcome measures (5)
- Change in growth rate (height velocity standard deviation score, HV SDS) [Time frame: From baseline (month 0) to end of study (up to 10 years)]
- Change in growth rate (HV SDS) between visits (usually patients are seen every 3 to 6 months) [Time frame: From baseline (month 0) to end of study (up to 10 years)]
- Adherence response as indicated in question at the bottom of newly developed Patient Reported Outcome (PRO) questionnaire each time questionnaire is filled out (preferably at each visit) [Time frame: From baseline (month 0) to end of study (up to 10 years)]
- Adherence measured as number of medication devices returned versus number of prescribed devices for the period between visits [Time frame: From baseline (month 0) to end of study (up to 10 years)]
- Change of self-rated adherence level throughout the study measured in newly developed PRO questionnaire each time questionnaire is filled out (preferably at each visit) [Time frame: From baseline (month 0) to end of study (up to 10 years)]
Eligibility criteria
Inclusion criteria
- Informed consent of parent or legally acceptable representative of subject and child assent, as age-appropriate must be obtained before any study-related activities.
- The parent or legally acceptable representative of the child must sign and date the Informed Consent Form (according to local requirements) and
- The child must sign and date the Child Assent Form or provide oral assent (if required according to local requirements).
- The decision to initiate treatment with commercially available Norditropin® FlexPro® has been made by the treating physician and the patient's parents/legal guardian before and independently of the decision to include the patient in this study.
- Male or female, all age groups equal to or below 15 years with more than 2 years expected remaining treatment time until reaching NFH. Patients who self-inject should be above 8 years of age in order to be able to fill in the questionnaire.
- Children being GH naïve at baseline with one of the following confirmed diagnoses
- Isolated growth hormone deficiency (iGHD)
- Small for gestational age (SGA)
Exclusion criteria
- Previous participation in this study. Participation is defined as having given informed consent in this study.
- Mental incapacity, unwillingness or language barriers precluding adequate understanding or cooperation.
- Patients who have an expected future duration of therapy of less than 2 years are not eligible for the study.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Germany · 1 center
- Uniklinik Ulm - Dt. Zentrum für Kinder- und Jugendgesundheit (DZKJ) — Ulm
Identifiers
NCT: NCT03972345 · GH-4488 · U1111-1217-5835