Cure My Disease

Don't miss your cure!

Home News Browse Soon ready About
Log in / Sign up

Congenital secretory sodium diarrhea 3

MONDO:0010036

Any secretory diarrhea in which the cause of the disease is a mutation in the SPINT2 gene.

Also known as: SPINT2 secretory diarrhea, SPINT2 secretory diarrhoea, congenital secretory sodium diarrhea type 3, congenital secretory sodium diarrhoea type 3, secretory diarrhea caused by mutation in SPINT2, secretory diarrhoea caused by mutation in SPINT2, DIAR3, diarrhea 3, secretory sodium, congenital, syndromic

3 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Disease (680) Hereditary disease (176) Digestive system disorder (160) Diarrheal disease (74) Human disease (14) Disease of genetic or genomic mechanism (2) Congenital diarrhea (0) Congenital secretory diarrhea (0) Congenital sodium diarrhea (0) Disease by body system or component (0)
Trials to join now! 1 Not yet recruiting 1 Completed 1
Sort by
  • Can a postbiotic soothe diarrhea in vulnerable kids?

    Symptom relief Not yet recruiting

    This trial is testing whether a postbiotic supplement called Lactobacillus LB (Lactéol®) is safe for hospitalized children under 18 with weakened immune systems who have diarrhea. Participants receive the supplement twice daily for 14 to 28 days alongside standard rehydration and…

    Phase: PHASE1, PHASE2 • Sponsor: Hospital Infantil de Mexico Federico Gomez • Aim: Symptom relief

    Last updated Aug 13, 2026 00:00 UTC

Cure My Disease

Helping patients find clinical trials that match their disease.

Why was Cure my disease built?

Explore

Home News Browse About Terms of use Contact us

This is a site from Cyber and Space