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Curcumin Supplementation as an Add on Treatment for Patients With Inflammatory Bowel Diseases Treated With Vedolizumab

Primary Purpose

Inflammatory Bowel Diseases

Status
Unknown status
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
Curcumin
Placebo
Sponsored by
Henit Yanai
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Inflammatory Bowel Diseases

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Established inflammatory bowel disease
  2. Age ≥18 years old
  3. At inclusion all patients must have a documented active colonic involvement based on either endoscopy or imaging:
  4. Commencing vedolizumab therapy according to the treating physician or on active therapy up to 6-weeks.
  5. Active luminal disease:

    CD- HBI ≥325, 26 UC- partial Mayo ≥227

  6. Evident active disease on endoscopy or imaging within 2-week from inclusion or elevated inflammatory markers at screening (CRP> 0.5 mg/dl, or fecal calprotectin>100 μgr/gr stool or ESR >40).

Exclusion Criteria:

  1. CD- isolated small bowel disease (L1) UC- proctitis (E1)
  2. Perianal disease
  3. Pregnancy
  4. Biliary obstruction
  5. Concomitant treatment with beta blockers, anti-coagulants, and norfloxacin (relative contra indications to curcumin therapy).
  6. Curcumin supplementations within the last 6 months.

Sites / Locations

  • Rabin Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Active

Sham

Arm Description

4 gr Curcumin daily for 1 year in addition to vedolizumab 300 mg per infusion (standard of care)

4 gr placebo daily for 1 year in addition to vedolizumab300 mg per infusion (standard of care)

Outcomes

Primary Outcome Measures

Clinical remission- Crohn's disease patients
Crohn's disease patients - disease activity indexe: Harvey Bradshow index (HBI) less that 3
Clinical remission- ulcerative colitis patients
Disease activity index - partial Mayo score less than 2

Secondary Outcome Measures

Disease response- Crohn's disease patients
Disease activity index- Harvey Bradshow index (HBI ) a drop of 3 points
Disease response- ulcerative colitis patients
Disease activity index -partial Mayo score a drop of 2 points
Biochemical remission
Fecal calprotectin less than 150 µg/gr
Biochemical remission
C reactive protein (CRP) less thn 0.5 mg/dl

Full Information

First Posted
June 14, 2017
Last Updated
October 7, 2020
Sponsor
Henit Yanai
Collaborators
Shaare Zedek Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT03500653
Brief Title
Curcumin Supplementation as an Add on Treatment for Patients With Inflammatory Bowel Diseases Treated With Vedolizumab
Official Title
Curcumin Supplementation as an Add on Treatment for Patients With Inflammatory Bowel Diseases Treated With Vedolizumab
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Unknown status
Study Start Date
June 9, 2020 (Actual)
Primary Completion Date
December 2021 (Anticipated)
Study Completion Date
December 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Henit Yanai
Collaborators
Shaare Zedek Medical Center

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
Introduction: The pathogenesis of inflammatory bowel diseases (IBD) is characterized by dysregulation of the innate immune response it's associated with Th1, Th17 up-regulation, reflected by increased cytokine secretion including TNF-α. A main effective therapeutic interventions is blocking TNFα. Vedolizumab, an anti integrin, is a new class of treatment designed to block trafficking of lymphocytes in the gut. Clinical trials and real life experience response rates at week 6 range between 30-45%. Curcumin suppresses NFκβ levels via alteration of TLR2/4 pathways lowering TNF-α upstream. Curcumin is safe and efficacious in inducing response and remission in mild-moderate Ulcerative colitis (UC) and maintaining remission when used as an add-on to 5ASA derivatives, only with strict adherence to treatment overtime. Objectives: Facing the low rate of response to therapies in IBD, the need for new treatments and the use of combination strategies lead us to believe that combining vedolizumab and curcumin may have a synergistic effect and will enable optimal immunomodulation. Hypothesis: Concomitant oral curcumin in IBD patients with colonic involvement will augment remission rates as well as clinical and biochemical response. Type of research and methods of data collection: A randomized controlled trial in 84 adults with colonic IBD (UC and CD). Eligible patients are during vedolizumab induction, patients will randomized will be into curcumin or placebo. Data will managed by investigators.

6. Conditions and Keywords

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

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Active
Arm Type
Active Comparator
Arm Description
4 gr Curcumin daily for 1 year in addition to vedolizumab 300 mg per infusion (standard of care)
Arm Title
Sham
Arm Type
Placebo Comparator
Arm Description
4 gr placebo daily for 1 year in addition to vedolizumab300 mg per infusion (standard of care)
Intervention Type
Dietary Supplement
Intervention Name(s)
Curcumin
Intervention Description
4 gr curcumin
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
4 gr placebo
Primary Outcome Measure Information:
Title
Clinical remission- Crohn's disease patients
Description
Crohn's disease patients - disease activity indexe: Harvey Bradshow index (HBI) less that 3
Time Frame
52 weeks
Title
Clinical remission- ulcerative colitis patients
Description
Disease activity index - partial Mayo score less than 2
Time Frame
52 weeks
Secondary Outcome Measure Information:
Title
Disease response- Crohn's disease patients
Description
Disease activity index- Harvey Bradshow index (HBI ) a drop of 3 points
Time Frame
52 weeks
Title
Disease response- ulcerative colitis patients
Description
Disease activity index -partial Mayo score a drop of 2 points
Time Frame
52 weeks
Title
Biochemical remission
Description
Fecal calprotectin less than 150 µg/gr
Time Frame
52 weeks
Title
Biochemical remission
Description
C reactive protein (CRP) less thn 0.5 mg/dl
Time Frame
52 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Established inflammatory bowel disease Age ≥18 years old At inclusion all patients must have a documented active colonic involvement based on either endoscopy or imaging: Commencing vedolizumab therapy according to the treating physician or on active therapy up to 6-weeks. Active luminal disease: CD- HBI ≥325, 26 UC- partial Mayo ≥227 Evident active disease on endoscopy or imaging within 2-week from inclusion or elevated inflammatory markers at screening (CRP> 0.5 mg/dl, or fecal calprotectin>100 μgr/gr stool or ESR >40). Exclusion Criteria: CD- isolated small bowel disease (L1) UC- proctitis (E1) Perianal disease Pregnancy Biliary obstruction Concomitant treatment with beta blockers, anti-coagulants, and norfloxacin (relative contra indications to curcumin therapy). Curcumin supplementations within the last 6 months.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Henit Yanai, MD
Phone
+972-3977241
Ext
5
Email
henitya@clalit.org.il
First Name & Middle Initial & Last Name or Official Title & Degree
Tamar Pfeffer-Gik, RD
Phone
+972-50-8864740
Email
tamarpf@clalit.org.il
Facility Information:
Facility Name
Rabin Medical Center
City
Petah tikva
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Henit Yanai, MD
First Name & Middle Initial & Last Name & Degree
Tamar Pfefer Gic, MA

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Curcumin Supplementation as an Add on Treatment for Patients With Inflammatory Bowel Diseases Treated With Vedolizumab

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