Actively Recruiting
Hypogonadotrophic Hypogonadism in Genetic Neurodevelopmental Conditions
Led by University of Sheffield · Updated on 2025-07-03
50
Participants Needed
1
Research Sites
224 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Hypogonadism is the medical name for a condition in which levels of the hormones which control sexual development are lower than normal. There are dozens of different causes of hypogonadism. Many people with hypogonadism have a change in a gene. There are many genes that give instructions for the hormones important for sexual development. Changes in one of these genes that stops the gene from working, can cause hypogonadism. In some of these medical conditions, there are additional features such as learning problems. In this study we will search databases to find all the genetic conditions that can be associated with hypogonadism. We will ask a number of people with changes in certain genes, identified from our search, to come to our research clinic. We will ask them about their health and examine them for signs of hypogonadism. For some, we will take blood samples to test for hypogonadism. This project will help us understand how common hypogonadism is, in people with these genetic changes, which will help with their treatment.
CONDITIONS
Official Title
Hypogonadotrophic Hypogonadism in Genetic Neurodevelopmental Conditions
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pathogenic SNV or CNV in neurodevelopmental disorders gene of interest
- Parent or carer consents to study
You will not qualify if you...
- Parent or carer does not consent to study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Sheffield Childrens Hospital NHS Foundation Trust
Sheffield, Select, United Kingdom, S11 9LE
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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