Research for Pathophysiology of Cancer Related Fatigue (CRF) and Chronic Fatigue (CFS/ME) (IMPROFA)
Primary Purpose
Cancer Related Fatigue, Fatigue Syndrome, Chronic
Status
Recruiting
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Probiotics
Placebo
Sponsored by
About this trial
This is an interventional basic science trial for Cancer Related Fatigue focused on measuring Cancer Fatigue, Chronic Fatigue
Eligibility Criteria
Inclusion Criteria:
- histologically, cytologically or radiologically confirmed tumor disease
- indication for chemotherapy
- Written consent to participation
Exclusion Criteria:
- chronic-inflammatory bowel disease
- pregnancy
Sites / Locations
- Saarland University Medical CenterRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Active Comparator
Placebo Comparator
Active Comparator
Placebo Comparator
Arm Label
Arm 1: Tumor disease w/o fatigue
Arm 2: Tumor disease w/o fatigue
Arm 3: Healthy control group
Arm 4: Healthy control group
Arm Description
Group receiving probiotics.
Group receiving placebo (corn starch)
Group receiving probiotics
Group receiving placebo (corn starch)
Outcomes
Primary Outcome Measures
Improvement of fatigue symptoms
Improvement of fatigue as measured by validated psychometric questionnaires.
Secondary Outcome Measures
Full Information
NCT ID
NCT03773003
First Posted
December 10, 2018
Last Updated
April 11, 2023
Sponsor
University Hospital, Saarland
1. Study Identification
Unique Protocol Identification Number
NCT03773003
Brief Title
Research for Pathophysiology of Cancer Related Fatigue (CRF) and Chronic Fatigue (CFS/ME)
Acronym
IMPROFA
Official Title
Pathophysiology of Cancer Related Fatigue (CRF) and Chronic Fatigue (CFS/ME) by Lipidomics, Metabolomics, Microbiome and Exome Analysis and Investigation of Clinical Improvement Under Administration of Probiotics
Study Type
Interventional
2. Study Status
Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 20, 2021 (Actual)
Primary Completion Date
November 1, 2024 (Anticipated)
Study Completion Date
December 1, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital, Saarland
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Research for Pathophysiology of Cancer Related Fatigue (CRF) and Chronic Fatigue Syndrome (CFS/ME) by Lipidomics, Metabolomics, Intestinal and Peritoneal Microbiome Analysis and Exome Analysis and Investigation of a Possible Benefit of Probiotics.
Detailed Description
This study aims to identify the underlying pathophysiology of Cancer Related Fatigue (CRF) by screening lipidome, metabolome, exome and microbiome of affected patients with tumor disease with and without fatigue. These results will be compared to an age- and gender matched control group with a comparable tumor disease and to another age- and gender matched control group without tumor disease.
The investigators are following the same strategy for investigating an underlying pathophysiology of Chronic Fatigue Syndrome (CFS/ME) in another group of patients. The age- and gender matched control group will be established from the beforementioned control group.
The investigators will also be screening for a peritoneal microbiome (possible correlate for leaky gut) in study patients undergoing abdominal surgery.
We will also investigate changes in fatigue and in lipidome, metabolome, exome and microbiome by double-blinded, placebo-controlled administration of probiotics to the study population.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cancer Related Fatigue, Fatigue Syndrome, Chronic
Keywords
Cancer Fatigue, Chronic Fatigue
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Double blinded, placebo controlled intervention with probiotics
There are three groups in the study:
Tumor disease with fatigue
Tumor disease without fatigue
Healthy control group
Masking
Investigator
Masking Description
Blinding will be made at the probiotics manufacturer's establishment. Neither investigators nor care providers nor patients know their status til the end of the study.
Allocation
Randomized
Enrollment
150 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Arm 1: Tumor disease w/o fatigue
Arm Type
Active Comparator
Arm Description
Group receiving probiotics.
Arm Title
Arm 2: Tumor disease w/o fatigue
Arm Type
Placebo Comparator
Arm Description
Group receiving placebo (corn starch)
Arm Title
Arm 3: Healthy control group
Arm Type
Active Comparator
Arm Description
Group receiving probiotics
Arm Title
Arm 4: Healthy control group
Arm Type
Placebo Comparator
Arm Description
Group receiving placebo (corn starch)
Intervention Type
Dietary Supplement
Intervention Name(s)
Probiotics
Intervention Description
The administered probiotics are readily available on the market and contain
Bifidobacterium breve, B. infantis, B. lactis, B. longum
Lactobacillus acidophilus, L. bulgaricus, L. casei, L. crispatus, L. fermentum, L. paracasei, L. plantarum, L. reuteri, L. rhamnosus, L. salivarius
Streptococcus thermophilus
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Identically looking to verum, containing corn starch.
Primary Outcome Measure Information:
Title
Improvement of fatigue symptoms
Description
Improvement of fatigue as measured by validated psychometric questionnaires.
Time Frame
3 months after end of chemotherapy
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
histologically, cytologically or radiologically confirmed tumor disease
indication for chemotherapy
Written consent to participation
Exclusion Criteria:
chronic-inflammatory bowel disease
pregnancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Michael Jelden, MD
Phone
+4968411630000
Email
michael.jelden@uks.eu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Jelden, MD
Organizational Affiliation
University Hospital, Saarland
Official's Role
Principal Investigator
Facility Information:
Facility Name
Saarland University Medical Center
City
Homburg
State/Province
Saarland
ZIP/Postal Code
66424
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Michael Jelden, Dr.
Phone
+49684116
Ext
30000
Email
michael.jelden@uks.eu
First Name & Middle Initial & Last Name & Degree
Michael Jelden, Dr.
Phone
49684116
Ext
15000
Email
michael.jelden@uks.eu
First Name & Middle Initial & Last Name & Degree
Michael Jelden, Dr.
12. IPD Sharing Statement
Learn more about this trial
Research for Pathophysiology of Cancer Related Fatigue (CRF) and Chronic Fatigue (CFS/ME)
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