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Gastrointestinal Motility in Patients With Neuroendocrine Tumors

Gastrointestinal Motility in Patients With Neuroendocrine Tumors-Effects of Sandostatin LAR

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00789841
Enrollment
13
Registered
2008-11-13
Start date
2008-09-30
Completion date
2010-05-31
Last updated
2010-10-26

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

Conditions

Neuroendocrine Tumor

Keywords

Neuroendocrine tumor, Carcinoid syndrome, Motility, Transit time

Brief summary

We will study the total gastrointestinal transit time (GITT), gastric emptying and small intestine motility in NET patients before and after treated with somatostatin analogues and compare these to healthy subjects. For this we will use radio-opaque markers and the newly developed Motility Tracking System (MTS). Hypothesis: Patients with NET and carcinoid syndrome have decreased GITT, gastric emptying and small bowel transit time and an increase in phase III MMC activity compared to healthy subjects. Treatment with somatostatin analogues increase transit times and decrease phase III MMC activity and improves the clinical symptoms.

Interventions

DEVICEMagnetic Tracking System (MTS) and radio-opaque markers

MTS: A small magnetic pill (6x15mm) is swallowed by the patient and the movement of this pill is registered by a sensor (coordinates x,y,z angles θ, φ) and depicted af graphs on a computer screen. For determination of GITT a capsule containing 10 radio-opaque markers is ingested every day for six days, on day seven an abdominal x-ray is performed.

Sponsors

Novartis
CollaboratorINDUSTRY
The Danish Medical Research Council
CollaboratorOTHER
University of Aarhus
Lead SponsorOTHER

Eligibility

Sex/Gender
ALL
Age
30 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* NET confirmed by histology * Diarrhea, (at least 3 loose or watery bowel movements per day) as part of carcinoid syndrome. * Newly referred patients without previous somatostatin analogue treatment or * NET patients who are pausing somatostatin analogue treatment due to other treatment or examination.

Exclusion criteria

* Subjects unable to understand the information * Severe diabetes with late complications or known metabolic disorder * Inflammatory bowel disease * Known clinically significant stenosis of the bowel * Bile acid malabsorption due to intestinal surgery * Small bowl bacterial overgrowth

Design outcomes

Primary

MeasureTime frame
Gastrointestinal transit time in NET patientsEnd of the study

Secondary

MeasureTime frame
Gastric emptying in NET patientsEnd of the study
Small intestinal transit timeEnd of the study
Small intestinal velocityEnd of the study
Changes in carcinoid symptoms and biomarkersEnd of the study

Countries

Denmark

Outcome results

None listed

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