A Multicenter Multinational Observational Study of Children With Hypochondroplasia
This study is for children with a specific genetic condition called hypochondroplasia. Researchers want to observe how these children grow and how their condition progresses over time. They will gather important information, such as height and other health measurements, to learn more about hypochondroplasia. The aim is to build a clearer picture of the condition's typical course, which could help doctors better support children and families in the future. It's an observational study, meaning participants will simply be monitored, and no new treatments will be given.
במבט חטוף
על מה המחקר הזה?
This study is looking into a genetic condition called hypochondroplasia, which can affect how children grow. It's a type of short stature, meaning children with the condition tend to be shorter than average. Because it's quite rare, doctors don't always have a full picture of how it affects children as they grow up.
The main goal of this study is to simply observe and understand the natural course of hypochondroplasia. This means researchers will follow children with the condition over time to see how their growth changes and what other health aspects might be important. They will collect measurements like height and other health-related information, but they won't be testing any new medicines or treatments.
Collecting this information is really important because it helps improve our understanding of hypochondroplasia. The more doctors know about how the condition typically develops, the better they can support families and provide the best possible care for children. Your participation would help build a better understanding for everyone affected by this condition.
נקודות עיקריות
- This study aims to understand how children with hypochondroplasia grow and develop.
- It's an observational study – no new medicines or treatments will be given.
- Participation involves regular check-ups and measurements of your child's growth.
- Only children aged 15 or under with a confirmed genetic diagnosis are eligible.
- Your child's information will help improve future understanding and care for hypochondroplasia.
מי עשוי להיות זכאי?
This study is for children aged 15 years or younger. To join, a child must have been officially diagnosed with hypochondroplasia through a genetic test. This test confirms the specific genetic change that causes the condition.
Children cannot join if they have another genetic condition that causes short height, apart from hypochondroplasia. Also, if a child has taken part in a study involving a new medicine or medical device within the last six months, they won't be able to join this study.
האם מחקר זה יכול להתאים לך?
ענה על השאלות המהירות הללו כדי לבדוק אם אתה עשוי להיות זכאי. זהו מדריך בלבד — צוות המחקר מקבל את ההחלטה הסופית.
- Is your child 15 years old or younger?
- Has your child been diagnosed with hypochondroplasia through a genetic test?
- Does your child have any other known genetic conditions causing short height (apart from hypochondroplasia)? (If yes, they might not be eligible)
- Has your child received any experimental medicine or device in the last 6 months? (If yes, they might not be eligible)
מה כרוך בהשתתפות?
If you decide to take part, your child will have their growth measured regularly, and other health information will be collected. This is an 'observational' study, which means no new medicines or treatments will be given as part of the study; your child will continue with their usual care. The visits will involve standard check-ups and measurements that would likely be part of their normal medical care. The study aims to follow children over time, but the exact number and timing of visits will be explained in full detail by the study team. You can stop participating at any time.
סיכונים ותועלות פוטנציאליים
מיקומים (43)
- בית החולים לילדים פיניקסמיקוד מאומתפניקס, ארצות הברית· גיוס
- Cedars-Sinai Medical Centerמיקוד מאומתלוס אנג'לס, ארצות הברית· עדיין לא מגייסים
- UCSF Benioff Children's Hospitalמיקוד מאומתאוקלנד, ארצות הברית· גיוס
- Nemours Alfred I. Dupont Hospital for Childrenמיקוד מאומתוילמינגטון, ארצות הברית· גיוס
- Children's National Health Systemמיקוד מאומתוושינגטון די.סי., ארצות הברית· גיוס
- בית החולים לילדים אן ורוברט ה. לורי בשיקגומיקוד מאומתשיקגו, ארצות הברית· גיוס
- The Johns Hopkins University School of Medicineמיקוד מאומתבולטימור, ארצות הברית· עדיין לא מגייסים
- Boston Children's Hospitalמיקוד מאומתבוסטון, ארצות הברית· גיוס
- University of Minnesota Masonic Children's Hospitalמיקוד מאומתמיניאפוליס, ארצות הברית· גיוס
- University of Missouriמיקוד מאומתColumbia, United States· גיוס
- Washington University School of Medicine in St. Louisמיקוד מאומתסנט לואיס, ארצות הברית· גיוס
- Mount Sinai Kravis Children's Hospitalמיקוד מאומתניו יורק, ארצות הברית· גיוס
שאלות נפוצות
What is hypochondroplasia?
It's a rare genetic condition that affects how bones grow, often leading to shorter stature.
Will my child receive new treatment in this study?
No, this is an observational study. Your child will continue with their current medical care; no new treatments are given.
How long will my child be in the study?
The study aims to follow children over time. The study team will give you details about the expected duration during your first visit.
Do we have to travel far for appointments?
This is a multicenter study, meaning it takes place in several locations. You would likely visit a research centre close to you. The study team can provide details.
Can I remove my child from the study?
Yes, you can choose to withdraw your child from the study at any time, for any reason, and it won't affect their medical care.
כיצד לגלות עוד
Trial Specialist
תמיד התייעץ עם רופא המשפחה או המומחה שלך לפני שתחליט להשתתף במחקר.
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