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Plant Exosomes +/- Curcumin to Abrogate Symptoms of Inflammatory Bowel Disease

Primary Purpose

Irritable Bowel Disease

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Sigmoidoscopy and biopsy, blood work
Sponsored by
University of Louisville
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Irritable Bowel Disease

Eligibility Criteria

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

Inclusion Criteria:

  • Patients must have a confirmed diagnosis of IBD (either CD or UC) with moderate disease activity.)
  • Ability to independently care for oneself

Exclusion Criteria:

  • Pregnancy
  • Known HIV
  • Patients receiving immunosuppressive drugs, other than for their bowel disease
  • Patients must be on stable doses of their medications for the 2 weeks prior to study entry and for the duration of the treatment period, or inform the investigator of any changes in medication
  • Active malignancy in the last 5 years
  • Patients receiving any other investigational agent(s)
  • Ginger allergy

Sites / Locations

  • University of Louisville

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Ginger exosomes

Curcumin

Ginger exosomes plus curcumin

Arm Description

Study mixture will be taken PO daily times 28 days Sigmoidoscopy and biopsy, blood work, quality of life questionnaire

Study mixture will be taken PO daily times 28 days Sigmoidoscopy and biopsy, blood work, quality of life questionnaire

Study mixture will be taken PO daily times 28 days Sigmoidoscopy and biopsy, blood work, quality of life questionnaire

Outcomes

Primary Outcome Measures

Change in inflammation on Colonoscopy
Decrease in inflammatory cells in the biopsy after treatment versus before treatment.

Secondary Outcome Measures

Change in Subjective symptoms
Questionnaire reporting of decrease in subjective symptoms.

Full Information

First Posted
June 6, 2018
Last Updated
November 2, 2022
Sponsor
University of Louisville
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1. Study Identification

Unique Protocol Identification Number
NCT04879810
Brief Title
Plant Exosomes +/- Curcumin to Abrogate Symptoms of Inflammatory Bowel Disease
Official Title
Pilot Clinical Trial Investigating the Ability of Plant Exosomes +/- Curcumin to Abrogate Symptoms of Inflammatory Bowel Disease (IBD)
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Completed
Study Start Date
March 1, 2018 (Actual)
Primary Completion Date
August 2, 2022 (Actual)
Study Completion Date
August 2, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Louisville

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 trial will test the hypothesis that edible structures within plant cells (ginger) will have clinically important anti-inflammatory effects on the gut lining of patients with inflammable bowel disease. To evaluate the safety and tolerability of exosomes with and without curcumin in patients with Inflammatory Bowel Disease (IBD); To estimate the effect of ginger exosomes or curcumin alone or combined with curcumin on the symptoms and disease score in patients with refractory IBD describe toxicities associated with ginger exosomes; to evaluate the effect of ginger exosomes on biomarkers of inflammation.
Detailed Description
Up to 90 patients with Chronic IBD will be enrolled, with the goal of having three arms of 30 subjects in each group who are eligible for evaluation. This exploratory trial is designed to estimate the effect of ginger exosomes or curcumin on IBD symptoms compared to ginger exosomes plus curcumin. In this prospective and randomized study the main focus is to compare exosomes alone, curcumin, and exosomes plus curcumin. Three primary stratification factors race (white and black), gender and type of IBD (CD and UC) will be used. plan Zelen's (1974) method will be used to avoid imbalance allocation within each stratum. A block size of 4 will be used. We plan to enroll all eligible patients visiting the clinic, as well as eligible patients referred from other gastroenterologists. All eligible visiting our clinic will be enrolled. By enrolling consecutive patients, we reduce selection bias. A patient will be enrolled only once. The most important aim of this study is to compare the IBD symptoms in exosomes alone and exosomes plus curcumin groups of patients. The symptomatology will be measured in each group and compared to the self-reported score. We will use the incidence rate of bloody stool to justify the sample size. With the combination treatment (ginger exosomes plus curcumin as compared to curcumin alone) we hope to reduce symptoms by at least 30%. Using a two sample one-sided t test for comparing mean differences in Inflammatory Bowel Disease Questionnaire, with 30 subjects in each group and using alpha=5%, we will have 80% power to detect effect size of 0.65 Standard Deviation, which is a large effect size (Cohen, 1988).. When the reduction in sample size due to missing data or other reasons, we will have reduced power to detect the difference in two groups.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Irritable Bowel Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
three Arms: 1. Ginger exosomes;2. Curcumin; 3. Ginger exosomes plus curcumin, Each PO daily times 28 days. All subjects will receive active treatment.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
4 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ginger exosomes
Arm Type
Active Comparator
Arm Description
Study mixture will be taken PO daily times 28 days Sigmoidoscopy and biopsy, blood work, quality of life questionnaire
Arm Title
Curcumin
Arm Type
Active Comparator
Arm Description
Study mixture will be taken PO daily times 28 days Sigmoidoscopy and biopsy, blood work, quality of life questionnaire
Arm Title
Ginger exosomes plus curcumin
Arm Type
Active Comparator
Arm Description
Study mixture will be taken PO daily times 28 days Sigmoidoscopy and biopsy, blood work, quality of life questionnaire
Intervention Type
Procedure
Intervention Name(s)
Sigmoidoscopy and biopsy, blood work
Other Intervention Name(s)
Inflammatory Bowel Disease Questionnaire
Intervention Description
Flexible tube up lower colon, blood draws, quality of life questionnaires
Primary Outcome Measure Information:
Title
Change in inflammation on Colonoscopy
Description
Decrease in inflammatory cells in the biopsy after treatment versus before treatment.
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Change in Subjective symptoms
Description
Questionnaire reporting of decrease in subjective symptoms.
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients must have a confirmed diagnosis of IBD (either CD or UC) with moderate disease activity.) Ability to independently care for oneself Exclusion Criteria: Pregnancy Known HIV Patients receiving immunosuppressive drugs, other than for their bowel disease Patients must be on stable doses of their medications for the 2 weeks prior to study entry and for the duration of the treatment period, or inform the investigator of any changes in medication Active malignancy in the last 5 years Patients receiving any other investigational agent(s) Ginger allergy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Susan Galandiuk, MD
Organizational Affiliation
University of Louisville
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Louisville
City
Louisville
State/Province
Kentucky
ZIP/Postal Code
40292
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
27318094
Citation
Zhang M, Viennois E, Prasad M, Zhang Y, Wang L, Zhang Z, Han MK, Xiao B, Xu C, Srinivasan S, Merlin D. Edible ginger-derived nanoparticles: A novel therapeutic approach for the prevention and treatment of inflammatory bowel disease and colitis-associated cancer. Biomaterials. 2016 Sep;101:321-40. doi: 10.1016/j.biomaterials.2016.06.018. Epub 2016 Jun 9.
Results Reference
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Plant Exosomes +/- Curcumin to Abrogate Symptoms of Inflammatory Bowel Disease

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