Panaceo "MED" for IBS (Irritable Bowel Syndrome) (PCeo-17)
Primary Purpose
Irritable Bowel Syndrome, Microbial Colonization, Intestinal Disease
Status
Completed
Phase
Not Applicable
Locations
Austria
Study Type
Interventional
Intervention
Zeolite
Sponsored by
About this trial
This is an interventional treatment trial for Irritable Bowel Syndrome focused on measuring Zeolite
Eligibility Criteria
Inclusion Criteria:
- Frequency of discomfort or pain in the abdomen in the last 3 months, more than 1 day per week.
- Start of the discomfort or pain more than 6 months ago.
- Improvement of the discomfort or pain associated with bowel movements sometimes, often, frequently, always.
- Association of the discomfort or pain with a frequency change in bowel movements sometimes, often, frequently, always.
- Association of the discomfort or pain with a change in stool-consistency sometimes, often, frequently, always.
Exclusion Criteria:
- Age: younger than 18, older than 80.
- Diagnosed inflammatory bowel disease (M. Crohn, Colitis Ulcerosa)
- Diagnosed nutritional idiosyncrasy
- Cancer treatment in the last 12 weeks
- Depression in the last 12 weeks
- Intake of weight loss supporting medication (Lipase inhibitors)
- Alcohol, nicotine, drug-abuse
- Status after organ-transplantation, intake of immunosuppressants
- Acute or chronic neurologic or psychiatric disease
- Acute or chronic heart disease or kidney disease
- Acute or chronic liver damage or any other organ damages
- Transient severe obstipation in the last 4 weeks
- Transient acute diarrhea in the last 4 weeks (e.g. intestinal infection)
- Intestinal cancer
- Intake of Panaceo MED or other Zeolite in the last 4 weeks
- Type I Diabetes or severe metabolic disease
- Infection with fever in the last 4 weeks
- Intake of cortisone or antibiotics in the last 4 weeks
- Planed journey of more than 14 days in the next 12 weeks (change of nutritional habits)
Sites / Locations
- SCIgenia GmbH
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Panaceo MED
Control
Arm Description
Zeolite, Medicinal product, class IIa for oral intake, daily intake of 2 sachets (3 g), for 3 months.
Micro crystalline cellulose daily intake of 2 sachets (3 g), for 3 months.
Outcomes
Primary Outcome Measures
Abdominal discomfort or pain
Frequency: 0 - never, 1 - less than once / month, 2 - once / month, 3 - two-three days / month, 4 - once per week, 5 - more than once per week, 6 - every day.
Symptom improvement with defaecation
0 - never or rarely, 1 - sometimes, 2 - often, 3 - frequently, 4 - always.
Stool frequency associated with abdominal discomfort or pain (more or less frequent)
0 - never or rarely, 1 - sometimes, 2 - often, 3 - frequently, 4 - always.
Stool consistency associated with abdominal discomfort or pain (softer or harder)
0 - never or rarely, 1 - sometimes, 2 - often, 3 - frequently, 4 - always.
Secondary Outcome Measures
Stool laboratory parameter: Firmicutes
Genotyping of bacteria in stool, before and after intake of study substance; Prevalence Firmicutes (CFU/g stool)
Stool laboratory parameter: Bacteroidetes
Genotyping of bacteria in stool, before and after intake of study substance; Prevalence Bacteroidetes (CFU/g stool)
Stool laboratory parameter: Ratio: Bacteroidetes/Firmicutes
Genotyping of bacteria in stool, before and after intake of study substance; Computation of Ratio: Bacteroidetes/Firmicutes
Stool laboratory parameter: Butyrat Producers
Genotyping of bacteria in stool, before and after intake of study substance; Prevalence of Butyratproducing bacteria (CFU/g stool)
Stool laboratory parameter: Clostridia
Genotyping of bacteria in stool, before and after intake of study substance; Prevalence of Clostridia (CFU/g stool)
Stool laboratory parameter: Histaminproducers,
Genotyping of bacteria in stool, before and after intake of study substance; Prevalence of Histaminproducing bacteria (CFU/g stool)
Stool laboratory parameter: H2S producers
Genotyping of bacteria in stool, before and after intake of study substance; Prevalence of H2S-producing bacteria (CFU/g stool)
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03817645
Brief Title
Panaceo "MED" for IBS (Irritable Bowel Syndrome)
Acronym
PCeo-17
Official Title
Pilot-trial on the Use of the Panaceo Medicine Product "MED" for the Treatment of IBS (Irritable Bowel Syndrome)
Study Type
Interventional
2. Study Status
Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
March 9, 2018 (Actual)
Primary Completion Date
June 30, 2019 (Actual)
Study Completion Date
June 30, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Scigenia GmbH
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Zeolite clinoptilolite is a volcanic mineral from the group of zeolites. The porous structure is associated with a large inner surface. Due to the anionic framework charge, ions (e.g., Pb^2+) can be absorbed or exchanged. The specific Panaceo PMA zeolite is approved as a class IIa medical device for the repair of the intestine inner lining. It is CE certified and complies with the relevant European Union regulations in terms of safety and effectiveness. Zeolite is known for its absorbing properties. Because of these properties and the results of several human studies, it warrants the investigation of possible effects on specific indications in human medicine, e.g. irritable bowel syndrome.
The diagnosis "irritable bowel syndrome (IBS)" is according to the ROME Foundation, an US medical society. IBS is a disorder with dysfunction of the bowels, a latent inflammation is discussed. The present study aims to evaluate the following effects in patients with IBS:
Primary endpoint: effect on the symptoms of IBS.
Secondary endpoint: intestinal wall permeability, integrity of the tight junctions as measured by the change in zonulin concentration in the stool.
Further endpoints:
Inflammation parameters and anti-inflammatory laboratory parameters.
Biodiversity of the gastrointestinal microbiome.
histamine-associated parameters.
Constipation as a possible side effect.
For this purpose, a double-blind randomized controlled trial (RCT) is realized prospectively in a monocentric outpatient-controlled study. The subjects take the test compound daily (verum, reference substance) for 12 weeks and document the intake of the study-substance, intake of medications, stool-frequency and consistency. They receive "before" and "after" the intervention phase a blood and stool analysis for the determination of parameters for intestinal wall integrity (zonulin) inflammation (hsCRP, interleukin-10, calprotectin), histamine metabolism, microbiome diversity. The pilot study is realized ahead of the detailed planning of a later main study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Irritable Bowel Syndrome, Microbial Colonization, Intestinal Disease
Keywords
Zeolite
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
41 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Panaceo MED
Arm Type
Experimental
Arm Description
Zeolite, Medicinal product, class IIa for oral intake, daily intake of 2 sachets (3 g), for 3 months.
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
Micro crystalline cellulose daily intake of 2 sachets (3 g), for 3 months.
Intervention Type
Other
Intervention Name(s)
Zeolite
Intervention Description
The natural zeolite clinoptilolite is of volcanic origin. The mineral belongs to the group of zeolite minerals. Zeolites are silicates with a microporous structure. This results in a stable structure with nanometer-sized cavities that pass through the natural zeolite clinoptilolite - comparable to a mineral sponge. Due to the numerous pores and channels, the mineral has a large internal surface and it can absorb molecules that are smaller in diameter than the pore openings. Since zeolite clinoptilolite has an anionic charge, there are cations such as Na +, K +, Ca 2+, Mg 2+ which can be exchanged for other ions (e.g., Pb^2+) in the cavities for electrical charge balance. In particular, the ion exchange capacity is essential for the effect and is used in many areas.
Primary Outcome Measure Information:
Title
Abdominal discomfort or pain
Description
Frequency: 0 - never, 1 - less than once / month, 2 - once / month, 3 - two-three days / month, 4 - once per week, 5 - more than once per week, 6 - every day.
Time Frame
3 months
Title
Symptom improvement with defaecation
Description
0 - never or rarely, 1 - sometimes, 2 - often, 3 - frequently, 4 - always.
Time Frame
3 months
Title
Stool frequency associated with abdominal discomfort or pain (more or less frequent)
Description
0 - never or rarely, 1 - sometimes, 2 - often, 3 - frequently, 4 - always.
Time Frame
3 months
Title
Stool consistency associated with abdominal discomfort or pain (softer or harder)
Description
0 - never or rarely, 1 - sometimes, 2 - often, 3 - frequently, 4 - always.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Stool laboratory parameter: Firmicutes
Description
Genotyping of bacteria in stool, before and after intake of study substance; Prevalence Firmicutes (CFU/g stool)
Time Frame
3 months
Title
Stool laboratory parameter: Bacteroidetes
Description
Genotyping of bacteria in stool, before and after intake of study substance; Prevalence Bacteroidetes (CFU/g stool)
Time Frame
3 months
Title
Stool laboratory parameter: Ratio: Bacteroidetes/Firmicutes
Description
Genotyping of bacteria in stool, before and after intake of study substance; Computation of Ratio: Bacteroidetes/Firmicutes
Time Frame
3 months
Title
Stool laboratory parameter: Butyrat Producers
Description
Genotyping of bacteria in stool, before and after intake of study substance; Prevalence of Butyratproducing bacteria (CFU/g stool)
Time Frame
3 months
Title
Stool laboratory parameter: Clostridia
Description
Genotyping of bacteria in stool, before and after intake of study substance; Prevalence of Clostridia (CFU/g stool)
Time Frame
3 months
Title
Stool laboratory parameter: Histaminproducers,
Description
Genotyping of bacteria in stool, before and after intake of study substance; Prevalence of Histaminproducing bacteria (CFU/g stool)
Time Frame
3 months
Title
Stool laboratory parameter: H2S producers
Description
Genotyping of bacteria in stool, before and after intake of study substance; Prevalence of H2S-producing bacteria (CFU/g stool)
Time Frame
3 months
Other Pre-specified Outcome Measures:
Title
Change of permeability (Leaky-Gut)
Description
Zonulin (< 55 ng/ml) in stool
Time Frame
3 months
Title
Change of bowel inflammation
Description
Calprotectin (< 50 mg/l) in stool
Time Frame
3 months
Title
Change of permeability of mucosa
Description
Alpha 1-Antitrypsin (< 27,5 mg/dl) in stool
Time Frame
3 months
Title
Change of the inflammation mediator
Description
Histamin (< 600 ng/ml) in stool
Time Frame
3 months
Title
Efficacy of binding and elimination of ammoniak
Description
Ammoniak (11-51 µmol/l) in blood / serum
Time Frame
3 months
Title
Change of inflammation
Description
high sensitivity C-reactive protein (mg/l) in blood / serum
Time Frame
3 months
Title
Change of anti-inflammatory mediator
Description
Interleukin-10 (< 9,1 pg/ml) in blood / serum
Time Frame
3 months
Title
Possible release of metal ions
Description
Aluminium (< 11 µg/l) in blood / serum
Time Frame
3 months
Title
Change of histamin metabolism
Description
Di-Amino-Oxydase (> 10 U/ml) in blood / serum
Time Frame
3 months
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:
Frequency of discomfort or pain in the abdomen in the last 3 months, more than 1 day per week.
Start of the discomfort or pain more than 6 months ago.
Improvement of the discomfort or pain associated with bowel movements sometimes, often, frequently, always.
Association of the discomfort or pain with a frequency change in bowel movements sometimes, often, frequently, always.
Association of the discomfort or pain with a change in stool-consistency sometimes, often, frequently, always.
Exclusion Criteria:
Age: younger than 18, older than 80.
Diagnosed inflammatory bowel disease (M. Crohn, Colitis Ulcerosa)
Diagnosed nutritional idiosyncrasy
Cancer treatment in the last 12 weeks
Depression in the last 12 weeks
Intake of weight loss supporting medication (Lipase inhibitors)
Alcohol, nicotine, drug-abuse
Status after organ-transplantation, intake of immunosuppressants
Acute or chronic neurologic or psychiatric disease
Acute or chronic heart disease or kidney disease
Acute or chronic liver damage or any other organ damages
Transient severe obstipation in the last 4 weeks
Transient acute diarrhea in the last 4 weeks (e.g. intestinal infection)
Intestinal cancer
Intake of Panaceo MED or other Zeolite in the last 4 weeks
Type I Diabetes or severe metabolic disease
Infection with fever in the last 4 weeks
Intake of cortisone or antibiotics in the last 4 weeks
Planed journey of more than 14 days in the next 12 weeks (change of nutritional habits)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ventzislav Petkov, M.D.
Organizational Affiliation
Physician
Official's Role
Principal Investigator
Facility Information:
Facility Name
SCIgenia GmbH
City
Vienna
ZIP/Postal Code
1090
Country
Austria
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
26500463
Citation
Lamprecht M, Bogner S, Steinbauer K, Schuetz B, Greilberger JF, Leber B, Wagner B, Zinser E, Petek T, Wallner-Liebmann S, Oberwinkler T, Bachl N, Schippinger G. Effects of zeolite supplementation on parameters of intestinal barrier integrity, inflammation, redoxbiology and performance in aerobically trained subjects. J Int Soc Sports Nutr. 2015 Oct 20;12:40. doi: 10.1186/s12970-015-0101-z. eCollection 2015.
Results Reference
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Panaceo "MED" for IBS (Irritable Bowel Syndrome)
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