Clin2
NCT02021604Possibly a fitRecruiting

Fluorodopa scan for congenital hyperinsulinism and insulinoma

Congenital HyperinsulinismInsulinoma

Part of Cancer, Digestive system, Genetic & congenital, Hormones & metabolism clinical trials.

This Phase 1 study tests a special imaging medicine (fluorodopa F 18) to help doctors better understand congenital hyperinsulinism (HI) patterns in the body. It may help guide treatment decisions to prevent dangerous low blood sugar and protect brain function.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1
Enrollment
250 people
Ages
Up to 18 years
Study type
Interventional

Who can take part

  • You or your child must have a confirmed diagnosis of congenital hyperinsulinism (HI)
  • Your HI specialist doctor must say standard medicines are not enough and surgery is recommended
  • Low blood sugar must have happened despite treatment, or fasting is not safe (can’t stay above 50 mg/dL for the required time)
  • Genetic test results should not clearly show a diffuse (widespread) HI type, or genetic results may be missing/negative
  • You must not be pregnant, and breastfeeding plans must allow stopping for 48 hours after the injection

View the official record on ClinicalTrials.gov

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Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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