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The Use of DPP-4 Inhibitors in Short Bowel Syndrome

The Use of Dipeptidyl Peptidase-4 Inhibitor Influences the Absorption of Intestine in Short Bowel Syndrome

Status
Terminated
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02653131
Acronym
DPP-4
Enrollment
8
Registered
2016-01-12
Start date
2016-01-31
Completion date
2020-04-30
Last updated
2020-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Short Bowel Syndrome

Keywords

Short bowel syndrome

Brief summary

The inhibition of Dipeptidyl peptidase-4 should increase the concentration of glucagone-like peptide 1 and 2, and the increase of the latter should increase the absorptive capacity of the intestine.

Detailed description

The only effective (to some extend drug) in short bowel syndrome is Glucacone-like peptide 4. Its price is, however, to high to really change the treatment strategy for intestinal failure. The Dipeptidyl peptidase-4 inhibitor, which a drug which is commonly used in the treatment of diabetes mellitus type II, should increase the concentration of glucagone-like peptide 1 and 2, and the increase of the latter should increase the absorptive capacity of the intestine.

Interventions

Sponsors

Stanley Dudrick's Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* patients receiving home parenteral nutrition (HPN) because of short bowel syndrome for at least 12 months * stable metabolic status * benign disease

Exclusion criteria

* HPN \< 12 months * metabolically unstable * cancer as the reason for intestinal failure

Design outcomes

Primary

MeasureTime frameDescription
Improvement of intestinal absorption12 monthsthe use of DPP-4 inhibitor results in the better intestinal absorption

Countries

Poland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026