Blood test may spare patients painful bone marrow biopsy
NCT ID NCT07562542
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study is testing whether a simple blood test can accurately diagnose systemic mastocytosis, a rare disease where too many mast cells build up in the body. Currently, diagnosis requires an invasive bone marrow biopsy. The blood test looks for a specific genetic mutation (KIT-D816V) using a highly sensitive method called ddPCR. If it works, it could make diagnosis easier and less painful for patients.
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 replace invasive bone marrow biopsies with a simple blood test for diagnosing systemic mastocytosis.
- What could go wrong
- This is a small, early-stage observational study with only 50 participants, so results may not apply to all patients. The blood test might not be as accurate as the standard biopsy.
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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.
Contacts and locations
Locations
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The First Affiliated Hospital of Soochow University, Jiangsu Institute of Hematology
RECRUITINGSuzhou, Jiangsu, 215000, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can biological signals explain mastocytosis symptoms?
- Experimental drug aims to tame rare mast cell disease
- Bone drug shows promise for rare mast cell disorder
- New antibody drug tested in patients with relapsed blood cancers
- New study screens for hidden genetic marker in mysterious mast cell disorders
- Old drug, new hope? thalidomide tested for rare mast cell cancer