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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03789136
Other study ID # NL58188.081.16
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 24, 2017
Est. completion date December 31, 2022

Study information

Verified date June 2021
Source Wageningen University
Contact Klaske van Norren, PhD
Phone +31317485790
Email klaske.vannorrren@wur.nl
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Rationale: Cancer cachexia is a complex metabolic syndrome characterized by clinically relevant loss of muscle mass with or without loss of fat mass. To determine how treatment methods can be most effective, full insight in changes in gene expression, body composition, muscle function and muscle metabolism are of great importance. Objective: Main aim of the study is to investigate the differences in gene expression, body composition, muscle function and muscle metabolism in colon cancer patients compared to controls. Study design: Observational study Study population: 40 colon cancer patients undergoing a tumor resection (30 primary tumor and 10 liver metastases) and 15 control patients undergoing an inguinal hernia repair (♂, 10) or an abdominal hysterectomy (♀, 5). Main study parameters/endpoints: Primary study parameter will be gene expression (transcriptomic and polymerase chain reaction analyses of muscle biopsies). Secondary parameters will be body composition (determined in available CT scans and bio impedance analysis and with DEXA), muscle function parameters (grip and knee flexion/extension strength and measured in a biopsy), metabolic markers (measured in fat and muscle biopsies), biochemical markers (measured in blood/serum) and gene expression of fat biopsies. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: The investigators expect no additional risk for the subjects due to the proposed measurements. Biopsies will be taken during the planned operation and therefore is not expected to cause a significant increase in burden for the patient. All other measurements are non-invasive, observational measurements with no risk of any harmful side effects.


Recruitment information / eligibility

Status Recruiting
Enrollment 55
Est. completion date December 31, 2022
Est. primary completion date December 31, 2022
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - CC patients: In order to be eligible to participate in this study, a subject must meet all of the following inclusion criteria: - Diagnosed with primary colon cancer (30) or liver metastases due to colon cancer(10) - Eligible for a primary tumor or liver metastases resection procedure - Controls: - Eligible for an inguinal hernia repair (?, 10) or an abdominal hysterectomy (?, 5) Exclusion Criteria: - CC patients: A potential subject who meets any of the following criteria will be excluded from participation in this study: - Having had chemotherapy or an operational procedure of the abdomen in the past 6 months - Suffering from malabsorption - Controls: - Having had treatment for previous or current tumors

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Not applicable, observational study
Not applicable, observational study

Locations

Country Name City State
Netherlands Gelderse Vallei Hospital Ede Gelderland

Sponsors (3)

Lead Sponsor Collaborator
Wageningen University Gelderse Vallei Hospital, Top Institute Food and Nutrition

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Muscle gene expression Muscle gene expression measured by microarray in a muscle biopsy taken from the rectus abdominis Biopsy during surgery
Secondary Body composition Measured using single slice staining of CT scan made for diagnostic purposes. Before surgery
Secondary Muscle function Measured using hand-grip strength Before surgery
Secondary Muscle protein metabolism Measured in a muscle biopsy taken from the rectus abdominis Biopsy during surgery
Secondary Adipose tissue gene expression Adipose tissue gene expression measured using PCR or micro-array in abdominal and subcutaneous fat Biopsy during surgery
Secondary Cytokine parameters in the blood Blood plasma cytokine levels measured using multiplex or similar technique Blood taken prior to surgery
Secondary Micro-nutrient parameters in the blood Micro-nutrient levels in the blood measured using LCMS, ELISA or similar techniques Blood taken prior to surgery
Secondary Cholesterol levels in the blood Cholesterol levels in the blood measured by GCMS Blood taken prior to surgery
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