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Clinical Research Directory

Browse clinical research sites, groups, and studies.

3 clinical studies listed.

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Short Gut Syndrome

Tundra lists 3 Short Gut Syndrome clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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ENROLLING BY INVITATION

NCT06240065

Successful Fiber Food Introduction in Short Bowel Syndrome

Short bowel syndrome (SBS) is a rare but challenging condition in which patients have insufficient bowel length to meet fluid, electrolyte, and nutrient requirements without parenteral support. The purpose of this study is to determine how well dietary fiber is tolerated in patients with or without short bowel syndrome based on assessment of gastrointestinal symptoms, weight, and corresponding changes in microbiome composition and metabolomics.

Gender: All

Ages: 4 Months - 17 Years

Updated: 2025-11-25

1 state

Short Gut Syndrome
ACTIVE NOT RECRUITING

NCT05432648

Fiber Food Introduction in Pediatric Short Bowel Syndrome

Short bowel syndrome (SBS) is a rare but challenging condition in which patients have insufficient bowel length to meet fluid, electrolyte, and nutrient requirements without parenteral support. The purpose of this study is to determine how well dietary fiber is tolerated in patients with short bowel syndrome compared to patients without short bowel syndrome based on assessment of gastrointestinal symptoms, and corresponding changes in microbiome composition and metabolomics.

Gender: All

Ages: 4 Months - 18 Years

Updated: 2025-08-17

1 state

Short Gut Syndrome
RECRUITING

NCT06904872

Safety and Efficacy of Crofelemer in Adult Patients With Short Bowel Syndrome and Intestinal Failure (SBS-IF) Without Colon-in-continuity (CIC)

A 24-week, randomized, placebo-controlled, double-blind study to evaluate the efficacy, safety and tolerability of crofelemer in patients with Short Bowel Syndrome and Intestinal Failure (SBS-IF) without colon-in-continuity (CIC) requiring parenteral support (PS). Blinded study drug will be administered orally (or enterally) three times daily (TID) as a novel crofelemer formulation, Crofelemer Powder for Oral Solution, or a matching placebo powder formulation for oral solution. Patients will be randomized in a 1:1:1 ratio to crofelemer 3 mg/kg/dose TID, crofelemer 10 mg/kg/dose TID or placebo and randomization will be stratified by baseline PS volume (≤4 or \>4 L/week).

Gender: All

Ages: 18 Years - Any

Updated: 2025-06-12

Short Bowel Syndrome
Malabsorption Syndromes
Short Gut Syndrome
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