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Intestinal permeability in cancer cachexia

Intestinal permeability in cancer cachexia - INSPIRE-X

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON57566
Enrollment
100
Registered
2024-12-21
Start date
2026-04-07
Completion date
Unknown
Last updated
2026-06-08

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

Conditions

cancer cachexia + cancer related weight loss

Interventions

n.a.

Sponsors

Universiteit Maastricht
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: To be eligible to participate in this study, a subject must meet all the  following criteria: • Age >= 18 years.  • Diagnosed with pancreatic cancer or colon cancer. • CT scan available. • Able to understand the Dutch language sufficiently to give informed consent  and follow orders during study procedures.  • Willingness to give informed consent. • Able to undergo gut permeability testing and functional muscle testing.

Exclusion criteria

Exclusion criteria: • Pancreatitis or inflammatory bowel disease. • Type I diabetes mellitus. • Peanut allergy. • Rye intolerance. • Chemotherapy in the past 8 weeks. • Large abdominal surgery in the past four weeks. • Total parenteral nutrition at day of surgery. • Systemic steroids or anti-inflammatory biologicals in the past two weeks. • Not able to perform physical activity. • Pregnant or lactating women. • Participation in possibly interfering studies within the last three months. • Inability to understand study information and/or communicate with staff.

Design outcomes

Primary

MeasureTime frame
The main study parameter is the difference in gut permeability index between cachectic and non-cachectic cancer patients. We will assess intestinal permeability through the sugar test, the peanut test, and supportive biomarkers like lipopolysaccharide binding protein (LBP), and intestinal fatty acid binding protein (iFABP).

Secondary

MeasureTime frame
• Changes in the spatial transcriptomes of cells supporting intestinal barrier function to gain a better understanding of metabolic alterations in the various cellular structures contributing to overall intestinal tissue. • Markers associated with: (I) muscle mass and functional decline, (II) immune system activity, (III) metabolism, (IV) bile acid signaling, and (V) gut-brain signaling, in both blood and tissue samples. • Alterations in the composition and metabolism of the gut microbiome.

Countries

Netherlands

Contacts

Public ContactS.S.M. Rensen

Universiteit Maastricht

s.rensen@maastrichtuniversity.nl+31 43 388 1499

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Jun 11, 2026