Tiny blood sample, big clues: stem cell study aims to unlock williams syndrome brain mystery
NCT ID NCT07537374
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study will collect blood from 3 children with Williams syndrome and 3 healthy children. Scientists will turn blood cells into stem cells and then into brain cells to study how the brain develops differently in Williams syndrome. The goal is to understand the disease better, not to test a treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could reveal how brain cells develop differently in Williams syndrome, pointing toward future targets for therapies.
- What could go wrong
- This is a very small, early-stage observational study with only 6 participants, so findings may not apply broadly. It is not testing any treatment.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 6 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Apr 2026
An estimate. Start dates often move.
- Expected to finish
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Jan 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The subjects of this study were children with Williams syndrome who were treated or followed up at Qilu Hospital of Shandong University, as well as healthy children recruited from the pediatric outpatient department during the same period. The study intends to collect peripheral blood samples from these children as subjects, establish a source-derived induced pluripotent stem cell (iPSC) line for the subjects, and use it for subsequent in vitro differentiation and mechanism research. It is planned to include 3 children with Williams syndrome and 3 healthy children, all of whom are independent donor-derived samples.
- Ages
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3 to 12 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. The clinical diagnosis is Williams syndrome. 2. Child subjects; 3. The guardian signs the informed consent form. If necessary, the subject himself/herself signs the informed consent or the informed consent with additional consent. 4. Be capable of completing peripheral blood collection; Exclusion Criteria: 1. Cases of severe infection, severe hematological diseases or other conditions that make blood collection inappropriate; 2. Recent receipt of special treatments that may significantly affect the state of peripheral blood cells; 3. Insufficient sample volume or poor sample quality that does not meet the requirements for reprogramming experiments; 4. Guardians' refusal to allow the samples to be used for iPSC establishment and subsequent research; 5. Other circumstances judged by the researchers as not suitable for inclusion in this study.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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