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Anti-Inflammatory Effects of Mango Polyphenolics in Inflammatory Bowel Disease

Primary Purpose

Intestinal Diseases, Ulcerative Colitis, Crohn Disease

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Mango polyphenolics
Sponsored by
Texas A&M University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Intestinal Diseases

Eligibility Criteria

18 Years - 72 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Male or female ages 18-79 years (see Protection of Human Subjects)
  • Treated with mesalamine or any mesalamine derivate, e.g.Asacol, Apriso, Asacol, Canasa, Lialda, Pentasa, Rowasa orally or rectally as standard of clinical care in the treatment of their symptoms for Inflammatory bowel disease
  • Treated using biologic immune-modulators including but not limited to: Infliximab, Adalimumab, Certolizumab, Natalizumab, azathioprine.
  • Additionally, patients may be on steroids (prednisone 10mg, budesonide 9mg)
  • Subjects must have been on a stable drug-regiment for at least 3 weeks before study begin.

Exclusion Criteria:

  • history of acute cardiac event, stroke, or cancer, within the last 6 months,
  • recurrent hospitalizations,
  • drug treatment of any of the listed conditions within the last 6 months,
  • abuse of alcohol or substance within the last 6 months,
  • currently smoking more than 1 pack/week,
  • seizures,
  • liver or renal dysfunction,
  • pregnancy or lactation,
  • allergy against mangos,
  • hepatitis B, C, or HIV,
  • regular exercise (>60 minutes, ≥ 5 times/wk), due to association of antioxidant and anti-inflammatory effects and moderate exercise.
  • known lactose intolerance, gluten sensitivity, or celiac disease
  • Patients that have upcoming Inflammatory bowel disease-related surgery and Inflammatory bowel disease -related intestinal stricture will also be excluded.

Sites / Locations

  • Texas A&M University, Clinical Lab, Nutrition and Food Science Department

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Mango

Arm Description

Mango polyphenolics

Outcomes

Primary Outcome Measures

Simple Clinical Colitis Activity Index (SCCAI)
A questionnaire used to assess the severity of symptoms in people who suffer from ulcerative colitis The score ranges from 0 to 19, where active disease is a score of 5 or higher compare changes in the score during the study

Secondary Outcome Measures

Short Inflammatory Bowel Disease Questionnaire (SIBDQ)
A health-related quality of life (HRQoL) tool measuring physical, social, and emotional status All scores were reported with a 7-point scale (Score 1-7, 1 = poor HRQOL, 7 = optimum HRQOL). compare changes in the score during the study
Biomarkers for inflammation : hs-CRP, Nf-kB, Il-6, Il-1b in Plasma (pg/ml)
- compare changes in the levels during the study

Full Information

First Posted
June 4, 2014
Last Updated
December 2, 2019
Sponsor
Texas A&M University
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1. Study Identification

Unique Protocol Identification Number
NCT02227602
Brief Title
Anti-Inflammatory Effects of Mango Polyphenolics in Inflammatory Bowel Disease
Official Title
The Mango Consumption Improves Biomarkers for Inflammation in Inflammatory Bowel Disease Patients
Study Type
Interventional

2. Study Status

Record Verification Date
December 2019
Overall Recruitment Status
Completed
Study Start Date
January 2014 (undefined)
Primary Completion Date
May 2017 (Actual)
Study Completion Date
March 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Texas A&M University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Bioactive compounds from mango are bioavailable and their anti-inflammatory efficacy has been demonstrated in animals and humans. However, the efficacy of mangoes has not previously been compared with respect to mild inflammatory bowel disease. In order to justify future pharmacokinetic and pharmacodynamic analyses in human clinical trials, a pilot assessment to determine efficacy in preventing or resolving Inflammatory bowel disease is a necessary step. Therefore, in this aim we will determine the clinical relevance of mango as an adjuvant treatment to conventional therapy in Inflammatory bowel disease . The effects of mango with common drug treatment in mild-moderate Inflammatory bowel disease will be compared to the drug-treatment alone. If mango or any other polyphenolic-rich food could be identified as helpful in shortening or reducing severity of episodes of inflammatory bowel disease, the addition of polyphenolics to conventional drug treatment in Inflammatory bowel disease would have a significant impact on public health.
Detailed Description
Rationale and Significance : Bioactive compounds from mango are bioavailable and their anti-inflammatory efficacy has been demonstrated in animals and humans. However, the efficacy of mangoes has not previously been compared with respect to mild inflammatory bowel disease. In order to justify future pharmacokinetic and pharmacodynamic analyses in human clinical trials, a pilot assessment to determine efficacy in preventing or resolving IBD is a necessary step. Therefore, in this aim we will determine the clinical relevance of mango as an adjuvant treatment to conventional therapy in IBD. The effects of mango with common drug treatment in mild-moderate IBD will be compared to the drug-treatment alone. If mango or any other polyphenolic-rich food could be identified as helpful in shortening or reducing severity of episodes of inflammatory bowel disease, the addition of polyphenolics to conventional drug treatment in IBD would have a significant impact on public health. The clinical study will be designed in subjects with mild-moderate active Crohn's disease (CD) or mild to moderate ulcerative colitis (UC). This study will be carried out with up to 8 weeks of mango treatment. Subjects with inflammatory bowel disease (IBD; CD or UC) will be performed at the Ertan Digestive Disease Center, Houston, TX, or Texas A&M University, College Station, TX. Patients may be recruited by advertisement (letters, emails, flyers, newspapers) or during standard of clinical care clinics: a) patients coming in for their regular, e.g. semi-annual or annual routine colonoscopy, b) UC or CD-related pain or symptoms, c) individuals presenting with diarrhoea that may be due to Crohn's disease or UC may also be recruited. Informed written consent will be obtained by the research personnel before the study begins. Approximately 90 individuals are expected to enroll in the study in order to obtain 60 subjects completing this study (considering screening failure and potential drop-outs). We expect a maximum of 90 subjects for the initial screening since many of these will be preselected from existing patient files. This study is designed to incorporate standard of care routine exams as performed within the division of gastroenterology. During the initial screening, the inclusion criteria of patients will be assessed using the clinical indices. it will be performed a screening in which above listed inclusion criteria and hemoglobin, and exclusion parameters and height, weight, calculation of BMI in kg/ (height in meters)2, albumin and C-reactive protein will be assessed due to the high correlation to IBD-activity (>45 mg/L). Subjects will be asked to give a stool sample that has to take place within 1 week before any endoscopic procedure is scheduled and laxatives are taken by the patients in preparation for the procedure. Study Treatments: Standard of clinical care + 200-400g of Mango b.i.d - t.i.d.,frozen or as smoothie. This study will be carried out as a pilot study with up to 8 weeks of mango treatment in addition to a list of standard of clinical care drugs. Subjects will be asked to record the exact amount consumed each day. Subjects who skip less than 1 day of mango consumption per week or less than 8 days over the entire period of 8 weeks of mango consumption will not be excluded from this study. Subjects will consume their regular diet but reduce the intake of plant-based dietary supplements which contain secondary plant compounds such as resveratrol, quercetin, tannins, and also reduce their carbohydrate-derived energy by the same amount which is supplied through their mango consumption. Patients that are not receiving the mango will consume their regular diet, which will be controlled for basic nutrients contained in the mango treatment. The mango treatment will start either on this first study day, or as soon as subjects can be classified within the inclusion criteria.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Intestinal Diseases, Ulcerative Colitis, Crohn Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Mango
Arm Type
Experimental
Arm Description
Mango polyphenolics
Intervention Type
Drug
Intervention Name(s)
Mango polyphenolics
Intervention Description
Frozen mango pack will be provided (200~400g per day).
Primary Outcome Measure Information:
Title
Simple Clinical Colitis Activity Index (SCCAI)
Description
A questionnaire used to assess the severity of symptoms in people who suffer from ulcerative colitis The score ranges from 0 to 19, where active disease is a score of 5 or higher compare changes in the score during the study
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Short Inflammatory Bowel Disease Questionnaire (SIBDQ)
Description
A health-related quality of life (HRQoL) tool measuring physical, social, and emotional status All scores were reported with a 7-point scale (Score 1-7, 1 = poor HRQOL, 7 = optimum HRQOL). compare changes in the score during the study
Time Frame
8 weeks
Title
Biomarkers for inflammation : hs-CRP, Nf-kB, Il-6, Il-1b in Plasma (pg/ml)
Description
- compare changes in the levels during the study
Time Frame
8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
72 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female ages 18-79 years (see Protection of Human Subjects) Treated with mesalamine or any mesalamine derivate, e.g.Asacol, Apriso, Asacol, Canasa, Lialda, Pentasa, Rowasa orally or rectally as standard of clinical care in the treatment of their symptoms for Inflammatory bowel disease Treated using biologic immune-modulators including but not limited to: Infliximab, Adalimumab, Certolizumab, Natalizumab, azathioprine. Additionally, patients may be on steroids (prednisone 10mg, budesonide 9mg) Subjects must have been on a stable drug-regiment for at least 3 weeks before study begin. Exclusion Criteria: history of acute cardiac event, stroke, or cancer, within the last 6 months, recurrent hospitalizations, drug treatment of any of the listed conditions within the last 6 months, abuse of alcohol or substance within the last 6 months, currently smoking more than 1 pack/week, seizures, liver or renal dysfunction, pregnancy or lactation, allergy against mangos, hepatitis B, C, or HIV, regular exercise (>60 minutes, ≥ 5 times/wk), due to association of antioxidant and anti-inflammatory effects and moderate exercise. known lactose intolerance, gluten sensitivity, or celiac disease Patients that have upcoming Inflammatory bowel disease-related surgery and Inflammatory bowel disease -related intestinal stricture will also be excluded.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Susanne Talcott, Ph.D
Organizational Affiliation
Texas A&M University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Texas A&M University, Clinical Lab, Nutrition and Food Science Department
City
College Station
State/Province
Texas
ZIP/Postal Code
77843
Country
United States

12. IPD Sharing Statement

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Anti-Inflammatory Effects of Mango Polyphenolics in Inflammatory Bowel Disease

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