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A Study of Chios Mastic Water in Irritable Bowel Syndrome (MASTIQUA)

Primary Purpose

Irritable Bowel Syndrome

Status
Completed
Phase
Not Applicable
Locations
Greece
Study Type
Interventional
Intervention
Chios mastic water
Placebo water
Chios mastic fruit juice
Placebo fruit juice
Sponsored by
Rutgers, The State University of New Jersey
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Irritable Bowel Syndrome focused on measuring Pistacia Lentiscus var. Chia, Chios mastic, mastiha, irritable bowel syndrome, dyspepsia, constipation, diarrhea, abdominal pain, bloating, gastrointestinal health

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age 18-65 years old
  2. Body mass index 18.5-35 kg/m2
  3. IBS diagnosis

Exclusion Criteria:

  1. Presence of other gastrointestinal disorders, such as gastritis, peptic ulcer, functional dyspepsia, celiac disease and inflammatory bowel disease
  2. Presence of other serious comorbidities, such as diabetes mellitus, active cancer, cardiovascular disease, pulmonary, kidney, liver, chronic inflammatory, autoimmune or psychiatric diseases
  3. Recent (within 6 months) surgery or hospitalization
  4. Habitual excessive alcohol consumption (> 210 or > 140 gr of alcohol per week for men and women, respectively)
  5. Currently on a weight-loss diet or recent change (within 6 months) in lifestyle habits
  6. Pregnancy or breast feeding (for women)

Sites / Locations

  • Department of Nutrition and Dietetics, School of Health Sciences and Education, Harokopio University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Placebo Comparator

Experimental

Placebo Comparator

Arm Label

Low-dose mastic group

Low-dose control group

High-dose mastic group

High-dose control group

Arm Description

This arm will consume 600 mL of a sparkling water enriched with Chios mastic per day for a 3-month period.

This arm will consume 600 mL of a standard sparkling water per day for a 3-month period.

This arm will consume 600 mL of a sparkling fruit juice enriched with Chios mastic per day for a 3-month period.

This arm will consume 600 mL of a standard sparkling fruit juice per day for a 3-month period.

Outcomes

Primary Outcome Measures

Change in IBS symptoms severity assessed through the IBS Symptom Severity Scale (IBS-SSS)
The score ranges from 0 to 500, with higher values indicating more severe symptoms.
Change in quality of life assessed through the IBS Quality of Life questionnaire (IBS-QOL)
Τhe score ranges from 34 to 170 with higher values indicating lower quality of life.

Secondary Outcome Measures

Change in high-sensitivity C-reactive protein
High-sensitivity C-reactive protein (mg/L) will be measured in blood samples by nephelometry.
Change in high-sensitivity interleukin-6 levels
High-sensitivity interleukin-6 levels (pg/mL) will be measured in blood samples using commercially available ELISA kits.
Change in malondialdehyde
Malondialdehyde levels (nmol/mL) will be measured in blood samples through HPLC-Fluorescence.
Change in total serum antioxidant capacity
Total serum antioxidant capacity (μmol/L) will be measured in blood samples using commercially available ELISA kits.

Full Information

First Posted
May 14, 2021
Last Updated
September 27, 2022
Sponsor
Rutgers, The State University of New Jersey
Collaborators
Harokopio University
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1. Study Identification

Unique Protocol Identification Number
NCT04893499
Brief Title
A Study of Chios Mastic Water in Irritable Bowel Syndrome
Acronym
MASTIQUA
Official Title
The Effectiveness of a Natural Aqueous Extract of Chios Mastic in the Management of Irritable Bowel Syndrome: the MASTIQUA Randomized Controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Completed
Study Start Date
September 12, 2021 (Actual)
Primary Completion Date
May 16, 2022 (Actual)
Study Completion Date
May 16, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rutgers, The State University of New Jersey
Collaborators
Harokopio University

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
Chios mastic is a natural product with strong antimicrobial, anti-inflammatory and antioxidant properties, and well-established benefits for dyspeptic disorders. The aim of the present study is to investigate the effectiveness of a natural aqueous extract of Chios mastic (mastic water), a by-product of Chios mastic processing, in the management of irritable bowel syndrome. This will be a 3-month randomized double-blind controlled clinical trial in adult patients with irritable bowel syndrome under standard medication. Participants will be blindly randomized to a low-dose mastic group, which will receive a carbonated water enriched with Chios mastic water (0.06%), a high-dose mastic group, which will receive a carbonated fruit juice enriched with Chios mastic water (0.55%), or one of the two control groups, which will receive an identical placebo water/fruit juice with no active ingredients. Participants will be evaluated in terms of anthropometric indices, lifestyle habits, severity of IBS-related gastrointestinal symptoms, quality of life, as well as biochemical, inflammatory and oxidative stress markers, both pre- and post-intervention.
Detailed Description
Chios mastic is the resin of the mastic tree (Pistacia Lentiscus var. Chia), produced exclusively in the southern part of the Greek island of Chios. References about its medical use from local populations for the treatment of gastrointestinal disorders or as a cosmetic agent can be found in ancient texts. Nowadays, this versatile resin has been rediscovered, not only as a traditional remedy and aromatic agent, but as a potent phytotherapeutic product with strong anti-inflammatory, anti-microbial and anti-oxidant properties. In 2015, Chios mastic was recognized as a herbal medicinal product by the European Medicines Agency (EMA), with two therapeutic indications: mild dyspeptic disorders and skin inflammation/healing of minor wounds (EMA/HMPC/46758/2015). Over the last years, Chios mastic is widely used in medicinal products, food supplements and cosmetics and has become the object of intense study in the fields of Nutrition and Pharmacotechnology. Irritable bowel syndrome (IBS) is a chronic functional gastrointestinal disease characterized by adverse changes in bowel function (frequency of bowel movements and/or stool composition) and abdominal pain. The clinical presentation of IBS usually includes symptoms of abdominal pain, flatulence, bloating, diarrhea and constipation that often alternate, while postprandial discomfort in the upper abdomen, feeling of fullness, nausea, vomiting and back pain are less commonly reported. IBS affects approximately 7-16% of the general population, and leads to reduced functionality and productivity and a significant deterioration in quality of life due to its various intestinal manifestations. The first-line pharmacological treatments for IBS aim at alleviating symptoms and include antispasmodics or anticonvulsants for abdominal pain, antidiarrheal medication and laxatives for constipation. Dietary modifications, such as the avoidance of foods that aggravate gastrointestinal symptoms and various types of exclusion diets, are also applied as adjunctive therapies for IBS management, but evidence of their effectiveness remains scares and inconclusive. The use of foods/beverages enriched with Chios mastic could constitute a promising complementary approach for the management of IBS, in combination with current first-line pharmacological treatments. The aim of the present interventional study is to explore the effectiveness of a natural aqueous extract of Chios mastic in the management of IBS. The study will be a 3-month parallel, randomized (allocation ratio 1:1), controlled, double-blind clinical trial in a sample of 60 adult patients with IBS. Eligible participants will be adult (18-65 years old) otherwise healthy individuals with an IBS diagnosis based on ROME IV criteria under stable medication. Participants will be excluded on the basis of the presence of other chronic gastrointestinal diseases, the presence of other serious comorbidities, or recent significant changes in lifestyle habits. Participants will be randomized to a low-dose mastic group (LDMG), a low-dose control group (LDCC), a high-dose mastic group (HDMG) or a high-dose control group (HDCC). The LDMG will be provided with 600 mL of a sparkling water (mastiqua) containing the natural mastic aqueous extract (0.06%) to be consumed daily (3 bottles of 200 mL each). The HDMG will be provided with 600 mL of a sparkling fruit juice (mastiqua lemon) containing the natural mastic aqueous extract (0.55%) to be consumed daily (3 bottles of 200 mL each). The LDCC and HDCC will receive the same quantity of a placebo sparkling water or fruit juice, respectively. For each type of drink (water and fruit juice), the intervention and placebo drinks will be unlabeled and identical in appearance and organoleptic characteristics, including the characteristic Chios mastic aroma. Randomization will be performed by an investigator with no clinical involvement, while all patients and study team members will be blinded to patient allocation in study groups. All enrolled patients will continue their standard medical treatment which must remain stable throughout the trial. The study physician will systematically record potential side-effects and will be in charge of terminating the intervention if needed. Participants will be assessed in terms of anthropometric indices (body weight, height, waist circumference, and body composition), lifestyle habits (diet and physical activity habits), the presence and severity of gastrointestinal symptoms, and quality of life both pre- and post-intervention. In addition, blood samples after a 12-hour fast and morning urine samples will be collected to measure biochemical, inflammatory and oxidative stress markers.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Irritable Bowel Syndrome
Keywords
Pistacia Lentiscus var. Chia, Chios mastic, mastiha, irritable bowel syndrome, dyspepsia, constipation, diarrhea, abdominal pain, bloating, gastrointestinal health

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
55 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Low-dose mastic group
Arm Type
Experimental
Arm Description
This arm will consume 600 mL of a sparkling water enriched with Chios mastic per day for a 3-month period.
Arm Title
Low-dose control group
Arm Type
Placebo Comparator
Arm Description
This arm will consume 600 mL of a standard sparkling water per day for a 3-month period.
Arm Title
High-dose mastic group
Arm Type
Experimental
Arm Description
This arm will consume 600 mL of a sparkling fruit juice enriched with Chios mastic per day for a 3-month period.
Arm Title
High-dose control group
Arm Type
Placebo Comparator
Arm Description
This arm will consume 600 mL of a standard sparkling fruit juice per day for a 3-month period.
Intervention Type
Behavioral
Intervention Name(s)
Chios mastic water
Other Intervention Name(s)
Mastiqua
Intervention Description
Participants randomized to this intervention arm will be provided with a sparkling water enriched with the natural mastic aqueous extract (0.06%), a by-product of Chios mastic processing, and will be asked to consume it daily (3 bottles of 200 mL each) for 3 months. Participants will also be instructed to keep the use of medication and dietary supplements stable and preserve their typical lifestyle habits throughout the study.
Intervention Type
Behavioral
Intervention Name(s)
Placebo water
Intervention Description
Participants randomized to this intervention arm will be provided with a standard sparkling water and will be asked to consume it daily (3 bottles of 200 mL each) for 3 months. Participants will also be instructed to keep the use of medication and dietary supplements stable and preserve their typical lifestyle habits throughout the study.
Intervention Type
Behavioral
Intervention Name(s)
Chios mastic fruit juice
Other Intervention Name(s)
Mastiqua lemon
Intervention Description
Participants randomized to this intervention arm will be provided with a sparkling fruit juice enriched with the natural mastic aqueous extract (0.55%), a by-product of Chios mastic processing, and will be asked to consume it daily (3 bottles of 200 mL each) for 3 months. Participants will also be instructed to keep the use of medication and dietary supplements stable and preserve their typical lifestyle habits throughout the study.
Intervention Type
Behavioral
Intervention Name(s)
Placebo fruit juice
Intervention Description
Participants randomized to this intervention arm will be provided with a standard sparkling fruit juice and will be asked to consume it daily (3 bottles of 200 mL each) for 3 months. Participants will also be instructed to keep the use of medication and dietary supplements stable and preserve their typical lifestyle habits throughout the study.
Primary Outcome Measure Information:
Title
Change in IBS symptoms severity assessed through the IBS Symptom Severity Scale (IBS-SSS)
Description
The score ranges from 0 to 500, with higher values indicating more severe symptoms.
Time Frame
0 (baseline) and 12 weeks
Title
Change in quality of life assessed through the IBS Quality of Life questionnaire (IBS-QOL)
Description
Τhe score ranges from 34 to 170 with higher values indicating lower quality of life.
Time Frame
0 (baseline) and 12 weeks
Secondary Outcome Measure Information:
Title
Change in high-sensitivity C-reactive protein
Description
High-sensitivity C-reactive protein (mg/L) will be measured in blood samples by nephelometry.
Time Frame
0 (baseline) and 12 weeks
Title
Change in high-sensitivity interleukin-6 levels
Description
High-sensitivity interleukin-6 levels (pg/mL) will be measured in blood samples using commercially available ELISA kits.
Time Frame
0 (baseline) and 12 weeks
Title
Change in malondialdehyde
Description
Malondialdehyde levels (nmol/mL) will be measured in blood samples through HPLC-Fluorescence.
Time Frame
0 (baseline) and 12 weeks
Title
Change in total serum antioxidant capacity
Description
Total serum antioxidant capacity (μmol/L) will be measured in blood samples using commercially available ELISA kits.
Time Frame
0 (baseline) and 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18-65 years old Body mass index 18.5-35 kg/m2 IBS diagnosis Exclusion Criteria: Presence of other gastrointestinal disorders, such as gastritis, peptic ulcer, functional dyspepsia, celiac disease and inflammatory bowel disease Presence of other serious comorbidities, such as diabetes mellitus, active cancer, cardiovascular disease, pulmonary, kidney, liver, chronic inflammatory, autoimmune or psychiatric diseases Recent (within 6 months) surgery or hospitalization Habitual excessive alcohol consumption (> 210 or > 140 gr of alcohol per week for men and women, respectively) Currently on a weight-loss diet or recent change (within 6 months) in lifestyle habits Pregnancy or breast feeding (for women)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Labros Sidossis, PhD
Organizational Affiliation
Department of Kinesiology and Health, School of Arts and Sciences, Rutgers University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Michael Georgoulis, PhD
Organizational Affiliation
Department of Nutrition and Dietetics, School of Health Sciences and Education, Harokopio University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Alexandra Karachaliou, MSc
Organizational Affiliation
Department of Nutrition and Dietetics, School of Health Sciences and Education, Harokopio University
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Nutrition and Dietetics, School of Health Sciences and Education, Harokopio University
City
Kallithea
State/Province
Attica
ZIP/Postal Code
17676
Country
Greece

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Deidentified individual participant data will be shared to investigators for the purpose of data meta-analysis, provided that the proposed use of the data has been approved by the Study Principal Investigator. Proposals should be directed to lsidossis@gmail.com. To gain access, data requestors will need to sign a data access agreement.

Learn more about this trial

A Study of Chios Mastic Water in Irritable Bowel Syndrome

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