Marine Protein Hydrolysate as Dietary Supplement in Irritable Bowel Syndrome (MPH_IBS)
Primary Purpose
Irritable Bowel Syndrome
Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
MPH_active
MPH_placebo
Sponsored by
About this trial
This is an interventional treatment trial for Irritable Bowel Syndrome focused on measuring Dietary Supplements, Fish Proteins, Protein Hydrolysates
Eligibility Criteria
Inclusion Criteria:
- Signed informed consent
- Body mass index (BMI) 18-30 kg/m2
- Irritable Bowel Syndrome (IBS) diagnosis according to Rome IV criteria
Exclusion Criteria:
- Suspected allergies against fish or shellfish
- Low or unstable blood pressure
- Diabetes mellitus pharmacologically treated
- Chronic diseases or therapies that are likely to interfere with the evaluation of study results such as known inflammation
- Acute infections (may be reconsidered for inclusion at a later time)
- Substance misuse
- Inability or unwillingness to comply with the requirements of study procedures
- Individuals in the middle of testing different dietary strategies for the treatment of IBS (such as the low-FODMAP diet) and/or not willing to/able to maintain a stable diet throughout the study period
- Use of pro- or prebiotic supplements
- Use of antibiotic treatment for the last 4 weeks
- Immunocompromised patient defined as taking immuno-suppressive medications
Sites / Locations
- Haukeland University Hospital
- Ålesund Hospital, Helse Møre og Romsdal HF
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
MPH_active
MPH_placebo
Arm Description
Daily intake at breakfast of supplementary marine protein hydrolysate (MPH). Random sequence of arms.
Daily intake at breakfast of supplementary placebo. Random sequence of arms.
Outcomes
Primary Outcome Measures
IBS-SSS
A decrease of 50 points or more in IBS-SSS, which is a clinically meaningful improvement.The IBS-SSS is a 5-question survey that asks the severity of abdominal pain, frequency of abdominal pain, severity of abdominal distention, dissatisfaction with bowel habits, and interference with quality of life over the past 10 days. Subjects respond to each question on a 100-point visual analogue scale. Scores on the IBS-SSS can range from 0 to 500 with higher scores indicating more severe symptoms. Subjects can be categorized as having mild (75-175), moderate (175-300), or severe (>300) IBS.
Secondary Outcome Measures
SF-NDI_HRQOL
The Short Form (SF) Nepean Dyspepsia Index is a 10-item questionnaire with 5 sub-scales each examining the influence of dyspepsia on domains of health in patients, namely tension/anxiety, interference with daily activities, disruption to regular eating/drinking, knowledge towards/control over disease symptoms and interference with work/study, with each sub-scale containing two items . Each item is measured by a 5-point Likert scale ranging from 0 (not at all or not applicable), 1 (a little), 2 (moderately), 3 (quite a lot) to 4 (extremely). Individual items in each sub-scale are aggregated to obtain a score range from 0 (lowest HRQoL score) to 100 (highest HRQoL score) as per the developers' original calculation formula. A total, overall SF-NDI total score is obtained using the mean of 5 subscale scores.
Fecal Calprotectin
Calprotectin is a protein found in several human fluids. When detected in the stool, calprotectin has a direct relationship (consequence of neutrophil degranulation) to inflammation in the bowel.
Full Information
NCT ID
NCT03801057
First Posted
January 9, 2019
Last Updated
August 12, 2019
Sponsor
Helse Møre og Romsdal HF
Collaborators
Haukeland University Hospital, University of Bergen
1. Study Identification
Unique Protocol Identification Number
NCT03801057
Brief Title
Marine Protein Hydrolysate as Dietary Supplement in Irritable Bowel Syndrome
Acronym
MPH_IBS
Official Title
The Effect of a Marine Protein Hydrolysate Supplement on Inflammatory Markers, Microbiota Composition and Symptoms in Patients With Irritable Bowel Syndrome
Study Type
Interventional
2. Study Status
Record Verification Date
August 2019
Overall Recruitment Status
Completed
Study Start Date
January 14, 2019 (Actual)
Primary Completion Date
March 21, 2019 (Actual)
Study Completion Date
April 21, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Helse Møre og Romsdal HF
Collaborators
Haukeland University Hospital, University of Bergen
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
The use of natural bioactive products for prevention and treatment of a wide spectrum of conditions, including gastrointestinal disorders and conditions is well known. Based on current evidences, the scientific validity of such products is limited. However, there is sufficient preliminary data to indicate that bioactive compounds may be novel for potentially clinical use, thus further clinical trials investigating effect are needed. This trial is meant to evaluate the effect of an marine protein hydrolysate (MPH) supplement on composition of microbiota, inflammatory markers and symptom severity in people diagnosed with irritable bowel syndrome.
Detailed Description
Previous studies performed in rodents have found that hydrolyzed proteins from fish alters the lipid and cholesterol metabolism, reduce plasma cholesterol and triglyceride levels and alters the fatty acid composition in liver and adipose tissue. Previous studies in humans have found marine peptides to have both antihypertensive and antioxidant effects. It is also suggested that fish protein hydrolysates may have an immunomodulating effect with beneficial properties in the intestine, and may prevent NSAID-induced injuries, change permeability in the gut and possibly prevent injurious conditions in the gut.
The evidence and knowledge are limited on the interaction between diet, gut microbiota and the influence of specific nutrients, as well as the impact of different sources of proteins on inflammation markers, gut microbiota and symptom severity in patients with irritable bowel syndrome (IBS). Different dietary sources of protein affect the diversity and composition of the human gut microbiota in different degree, demonstrated by a distinct gut bacteria profile observed between omnivores and vegetarians.The specific effect of marine peptides on human gut microbiota composition is as far as the investigators know, previously not investigated. Interestingly, novel results indicate that the presence of fish proteins in the diet have impact on both composition and activity of the gut microbiome, influencing the human microbiota composition.
The many benefits of expanding the utilization of marine products, the previous assumed beneficial intestinal effect and the increased interest in gut health and microbiota, as well as a great need for novel dietary treatment strategies for patients with irritable bowel syndrome (IBS) make this study warrant.
Aim with this trial is to evaluate the effect of an marine protein hydrolysate (MPH) supplement on composition of microbiota, inflammatory markers and symptom severity in human subjects diagnosed with IBS.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Irritable Bowel Syndrome
Keywords
Dietary Supplements, Fish Proteins, Protein Hydrolysates
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A parallel group randomized, controlled clinical trial for six weeks
Masking
ParticipantCare ProviderInvestigator
Masking Description
The provider of the dietary supplement deliver the supplement prepared and packed in equal bags (active/placebo) that we hand out to the participants in an randomized order.
Allocation
Randomized
Enrollment
40 (Actual)
8. Arms, Groups, and Interventions
Arm Title
MPH_active
Arm Type
Active Comparator
Arm Description
Daily intake at breakfast of supplementary marine protein hydrolysate (MPH). Random sequence of arms.
Arm Title
MPH_placebo
Arm Type
Placebo Comparator
Arm Description
Daily intake at breakfast of supplementary placebo. Random sequence of arms.
Intervention Type
Dietary Supplement
Intervention Name(s)
MPH_active
Intervention Description
One daily intake at breakfast of supplementary marine protein hydrolysate (MPH), a dosage of 2400 mg, duration 6 weeks. The form is powder, flavored with lemon, and to be mixed with 100 ml water. Random sequence of arms.
Intervention Type
Dietary Supplement
Intervention Name(s)
MPH_placebo
Intervention Description
One daily intake at breakfast of supplementary placebo, a dosage of 2400 mg, duration 6 weeks. The form is powder, flavored with lemon, and to be mixed with 100 ml water.
Primary Outcome Measure Information:
Title
IBS-SSS
Description
A decrease of 50 points or more in IBS-SSS, which is a clinically meaningful improvement.The IBS-SSS is a 5-question survey that asks the severity of abdominal pain, frequency of abdominal pain, severity of abdominal distention, dissatisfaction with bowel habits, and interference with quality of life over the past 10 days. Subjects respond to each question on a 100-point visual analogue scale. Scores on the IBS-SSS can range from 0 to 500 with higher scores indicating more severe symptoms. Subjects can be categorized as having mild (75-175), moderate (175-300), or severe (>300) IBS.
Time Frame
Before (baseline) and after intervention (6 weeks later).
Secondary Outcome Measure Information:
Title
SF-NDI_HRQOL
Description
The Short Form (SF) Nepean Dyspepsia Index is a 10-item questionnaire with 5 sub-scales each examining the influence of dyspepsia on domains of health in patients, namely tension/anxiety, interference with daily activities, disruption to regular eating/drinking, knowledge towards/control over disease symptoms and interference with work/study, with each sub-scale containing two items . Each item is measured by a 5-point Likert scale ranging from 0 (not at all or not applicable), 1 (a little), 2 (moderately), 3 (quite a lot) to 4 (extremely). Individual items in each sub-scale are aggregated to obtain a score range from 0 (lowest HRQoL score) to 100 (highest HRQoL score) as per the developers' original calculation formula. A total, overall SF-NDI total score is obtained using the mean of 5 subscale scores.
Time Frame
Before (baseline) and after intervention (6 weeks later).
Title
Fecal Calprotectin
Description
Calprotectin is a protein found in several human fluids. When detected in the stool, calprotectin has a direct relationship (consequence of neutrophil degranulation) to inflammation in the bowel.
Time Frame
Before (baseline) and after intervention (6 weeks later).
Other Pre-specified Outcome Measures:
Title
Inflammatory markers in blood
Description
Zonulin, iFABP (intestinal fatty acid binding protein), LBP (lipopolysaccharide binding protein), IL-4, 6, 8, 10, TNF-α and INF-γ are markers of bowel mucosal damage.
Time Frame
Before (baseline) and after intervention (6 weeks later).
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Signed informed consent
Body mass index (BMI) 18-30 kg/m2
Irritable Bowel Syndrome (IBS) diagnosis according to Rome IV criteria
Exclusion Criteria:
Suspected allergies against fish or shellfish
Low or unstable blood pressure
Diabetes mellitus pharmacologically treated
Chronic diseases or therapies that are likely to interfere with the evaluation of study results such as known inflammation
Acute infections (may be reconsidered for inclusion at a later time)
Substance misuse
Inability or unwillingness to comply with the requirements of study procedures
Individuals in the middle of testing different dietary strategies for the treatment of IBS (such as the low-FODMAP diet) and/or not willing to/able to maintain a stable diet throughout the study period
Use of pro- or prebiotic supplements
Use of antibiotic treatment for the last 4 weeks
Immunocompromised patient defined as taking immuno-suppressive medications
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dag Arne Lihaug Hoff, MD, PhD
Organizational Affiliation
Helse Møre og Romsdal Hospital Trust
Official's Role
Study Director
Facility Information:
Facility Name
Haukeland University Hospital
City
Bergen
Country
Norway
Facility Name
Ålesund Hospital, Helse Møre og Romsdal HF
City
Ålesund
Country
Norway
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
31319590
Citation
Dale HF, Jensen C, Hausken T, Valeur J, Hoff DAL, Lied GA. Effects of a Cod Protein Hydrolysate Supplement on Symptoms, Gut Integrity Markers and Fecal Fermentation in Patients with Irritable Bowel Syndrome. Nutrients. 2019 Jul 17;11(7):1635. doi: 10.3390/nu11071635.
Results Reference
result
Learn more about this trial
Marine Protein Hydrolysate as Dietary Supplement in Irritable Bowel Syndrome
We'll reach out to this number within 24 hrs