The Pathogenesis of Chronic Diarrhoea After Treatment for Cancer in Cecum and the Ascending Colon

Sponsor
University of Aarhus (Other)
Overall Status
Completed
CT.gov ID
NCT04003181
Collaborator
Danish Cancer Society (Other), GE Healthcare (Industry)
64
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43.9
1.5

Study Details

Study Description

Brief Summary

Many patients suffer from chronic diarrhoea after surgical treatment for cancer in the right side of the colon.

The investigators' main hypothesis is that colon cancer patients with chronic diarrhoea have a higher risk of bile acid malabsorption compared with colon cancer patients without diarrhoea.

The investigators also expect that a part of the cases of bile acid malabsorption is caused by underlying bacterial overgrowth in the small bowel.

The investigators assume that patients with severe bile acid malabsorption have a lower value of FGF19 in the blood compared to patients with moderate or none bile acid malabsorption.

Furthermore, it is assumed that patients with chronic diarrhoea and documented bile acid malabsorption after surgical treatment for right-sided colon cancer will get improved bowel function when treated with a bile acid binder, or antibiotics in case of bacterial overgrowth.

Condition or Disease Intervention/Treatment Phase
N/A

Detailed Description

Patients with chronic diarrhoea after surgical treatment of right-sided colon cancer will be compared to patients without diarrhoea after right-sided colon cancer treatment.

All patients will be asked to answer a short questionnaire regarding bowel function, and they will all have standard blood tests taken to exclude non-cancer related causes of diarrhoea. Besides these standard tests, the value of FGF19 will be measured in a blood sample from the fasting participants. All participants will undergo SeHCAT scan to determine the presence of bile acid malabsorption among right-sided colon cancer patients with and without diarrhoea. In addition, a glucose breath test will be performed to examine, if the patients have small intestinal bacterial overgrowth.

Patients with a positive glucose breath test, and thus bacterial overgrowth, will be treated with antibiotics, followed by another SeHCAT scan, glucose breath test, and measurement of gastrointestinal transit time. In addition, they will be asked to complete the questionnaire regarding bowel function again. All cases with an abnormal SeHCAT scan will be treated with a bile acid binder, and the patients will be asked to complete the questionnaire one more time, and the GITT measurement will be repeated.

Study Design

Study Type:
Interventional
Actual Enrollment :
64 participants
Allocation:
Non-Randomized
Intervention Model:
Factorial Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
The Pathogenesis of Chronic Diarrhoea After Treatment for Cancer in Cecum and the Ascending Colon
Actual Study Start Date :
Sep 28, 2017
Actual Primary Completion Date :
May 26, 2021
Actual Study Completion Date :
May 26, 2021

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Positive breath test

Patients with a positive breath test are treated with antibiotics.

Drug: Antibiotics
Ciprofloxacin or Rifaximin for 10 days.

Active Comparator: Positive SeHCAT scan

Patients with a positive SeHCAT scan are treated with a bile acid binder.

Drug: Bile Acid Binder
Cholestyramine or Colesevelam lifelong.

No Intervention: No intervention

Patients with a normal breath test and a normal SeHCAT scan receive no intervention.

Outcome Measures

Primary Outcome Measures

  1. Change in SeHCAT retention after 7 days. [The SeHCAT scan consists of a baseline measurement and a measurement after 7 days.]

    The diagnosis of bile acid malabsorption in cases vs. controls is determined by a positive SeHCAT scan.

  2. Serum concentration of FGF19 [Through study completion, an average of 1 month.]

    The serum value of FGF19 is measured by a blood sample.

Secondary Outcome Measures

  1. Presence of bacteria in the small bowel [Through study completion, an average of 1 month.]

    The diagnosis of bacterial overgrowth in the small bowel is determined by a breath test.

  2. Symptom relief after treatment with antibiotics or bile acid binder [After 3 months.]

    This will be estimated based on self-reported symptoms: A bowel function questionnaire with 30 questions regarding different aspects of bowel function. The patients should state if they have the symptoms daily, 1-6 times per week, less than once a week, or never.

  3. Quality of life after treatment with antibiotics or bile acid binder [After 3 months.]

    This will be estimated based on self-reported symptoms: the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire C30 version 3.0. A questionnaire with 30 individual questions summing up to form one global health status, five functional subscales, three symptom scales and six single items addressing different aspects of quality of life. The scales range from 0-100 with a higher score representing a higher level of functioning or a higher degree of symptoms, respectively.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Primary adenocarcinoma in cecum or the ascending colon

  • Right-sided hemicolectomy

  • Understanding, speaking and reading Danish

Exclusion Criteria:
  • Previous major gastrointestinal, urological or gynaecological surgery or oncological treatment

  • Radiation therapy

  • Recurrence of colon cancer

  • Metastasis

  • Permanent stoma

  • Pregnancy

  • Reduced cognitive level that makes it plausible that the patient do not understand the study or is not capable of participation

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Hepatology and Gastroenterology, Aarhus University Hospital Aarhus Denmark 8200

Sponsors and Collaborators

  • University of Aarhus
  • Danish Cancer Society
  • GE Healthcare

Investigators

  • Study Chair: Søren Laurberg, MD DMSc, Department of Surgery, Aarhus University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Aarhus
ClinicalTrials.gov Identifier:
NCT04003181
Other Study ID Numbers:
  • 1-10-72-301-16
  • 1-16-02-137-17
First Posted:
Jul 1, 2019
Last Update Posted:
Sep 8, 2021
Last Verified:
Aug 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Aarhus
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 8, 2021