Functional Sucrase Deficiency in Short Bowel Syndrome Patients With Intestinal Failure

• Status: Not yet recruiting
• Trial end date: 2022-11-01
• Target enrollment: 0
• Participant gender: All

Summary

Short gut syndrome with intestinal failure patients may have decreased production of disaccharidases, like sucrase, an enzyme responsible for digesting sugar in foods. This can happen due to loss of bowel length from surgery or from loss of cellular function in the intestines due to use of parenteral nutrition intravenously. Therefore, patients with these conditions may not be able to digest sucrose (sugar) fully. Patients might experience abdominal distension/pain, vomiting and diarrhea when sugar is taken in orally or through the g-tube, which can limit patients' ability to increase oral or g-tube feeds in short gut syndrome patients with intestinal failure.

In patients with short gut syndrome and intestinal failure, the administration of exogenous sucrase (enzyme) may improve sucrose (sugar) digestion and thus the ability to tolerate more oral or g-tube feeds.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: University of Miami
• Collaborator: QOL Medical, LLC

Criteria

Inclusion Criteria:

• Short bowel syndrome, of all ages, with dependence on parental support to provide at least 50% of fluid or caloric needs.

• Must be on diet containing sucrose.

• Must be willing and able to sign informed consent

• Adult and Pediatric patients (all ages)

Exclusion Criteria:

• Current IV antibiotic administration for confirmed bout of bacteremia.

• No enteral nutrition

• Any condition, disease, illness, or circumstance that in the investigator's opinion puts the subject at any undue risk, prevents completion of the study, or interferes with analysis of the study results