Clin2
NCT07627217Likely a fitRecruiting

Understanding MNGIE disease progression and natural history

MNGIEMitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE)

Part of Brain & nervous system, Digestive system, Genetic & congenital clinical trials.

This study collects information from patients with MNGIE (a rare genetic condition affecting how cells break down certain molecules) to better understand how the disease develops and progresses over time. By learning more about your experience, researchers hope to develop better treatments.

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

Phase
N/A
Enrollment
50 people
Ages
Any age
Study type
Observational

Who can take part

  • You have a confirmed diagnosis of TP deficiency (also called MNGIE), confirmed by genetic testing, enzyme levels, or specific blood markers
  • You can be any age, at any stage of disease, or even have had the condition previously
  • You may be included whether you have symptoms or not
  • The study accepts information about patients who have passed away
  • There are no other disqualifying conditions—all patients with confirmed TP deficiency are welcome

View the official record on ClinicalTrials.gov

Quick eligibility check

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

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