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Curcumin for Prevention of Relapse in Patients With Ulcerative Colitis

Primary Purpose

Ulcerative Colitis in Remission

Status
Terminated
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Curcumin
Placebo
Sponsored by
Chinese University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Ulcerative Colitis in Remission

Eligibility Criteria

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

Inclusion Criteria:

  • in clinical remission for at least 1 month, defined as Mayo bowel frequency subscore ≤ 1 and Mayo rectal bleeding subscore = 0 (Table 2).
  • a history of at least one flare with symptoms that required intervention within 24 months before screening
  • age ≥ 18
  • written informed consent obtained

Exclusion Criteria:

  • receipt of immunosuppressive drugs or corticosteroids within 60 days of screening
  • prior bowel surgery except appendectomy
  • with severe relapse (Mayo score 9-12) in the last 3 months
  • History or evidence of incompletely resected colonic mucosal dysplasia
  • on regular curcumin supplements or intake of curry in diet for ≥5 days each week
  • presence of infections (exclude simple infections such as influenza, etc.) or sepsis
  • pregnancy or lactating women
  • with a Mayo endoscopic subscore ≥2 on sigmoidoscopy or colonoscopy at baseline
  • allergic to curry-related products

Sites / Locations

  • Prince of Wales Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Curcumin

Curcumin Placebo

Arm Description

Dietary supplements of Curcumin capsules

Identical looking placebo of the active arm

Outcomes

Primary Outcome Measures

The relapse rate at 12 months
Defined as clinical symptoms (increased bowel frequency with a bowel frequency Mayo subscore ≥ 1 or rectal bleeding with a Mayo rectal bleeding subscore ≥ 1) together with endoscopic evidence of active disease (Mayo endoscopic subscore ≥ 2).

Secondary Outcome Measures

Adverse events
The severity grading of AEs will be assessed as Grade 1, 2, 3, 4 or 5 using the Common Terminology Criteria for Adverse Events (CTCAE) Version 4.03 Grading Scale, which can be found at: http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010-06-14_QuickReference_8.5x11.pdf
Endoscopic remission
Defined as a mayo endoscopic subscore of 0 or 1
Simple Clinical Colitis Activity Index (SCCAI)
compare the scores in two groups
Fecal calprotectin levels at 12 months
compare the difference of the levels between groups
Fecal immunochemical test (FIT) at 12 months
compare the positivity rate in those with flare
Quality of Life assessed by the Inflammatory Bowel Disease Questionnaire (IBDQ)
compare the scores in two groups
Patient Reported Outcomes (PRO) Questionnaire
The questionnaire will ask during the study follow up about the psychological aspects of UC patients, the baseline and score on final visit will be compared, as well as between the two groups
Pharmacokinetics study to measure the drug concentration-time courses
compare the absorption rate in two groups and to establish and evaluate the relationships and subsequently describe the effect-time courses of curcumin absorption in blood and colon.

Full Information

First Posted
April 7, 2017
Last Updated
October 13, 2022
Sponsor
Chinese University of Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT03122613
Brief Title
Curcumin for Prevention of Relapse in Patients With Ulcerative Colitis
Official Title
A Double-blind, Randomized, Placebo-Controlled Trial of Curcumin Versus Placebo for Prevention of Relapse in Patients With Ulcerative Colitis
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Terminated
Why Stopped
Decision made by team of investigators
Study Start Date
June 19, 2017 (Actual)
Primary Completion Date
May 22, 2020 (Actual)
Study Completion Date
May 22, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
UC is a chronic inflammatory bowel disorder with relapsing and remitting course. The efficacy of mesalazine in preventing relapse in patients with UC is well-known and supported by randomized studies. However, mesalazine can be associated with side-effects. In addition, drug compliance is suboptimal, especially when disease is not active. Curcumin is a natural phytochemical derived from the Indian spice turmeric. It is widely used, has potent anti-inflammatory, anti-oxidant and anti-tumour properties. The aims of this double-blind, placebo-controlled randomized trial is to assess the efficacy of curcumin in the prevention of relapse in patients with ulcerative colitis (UC).
Detailed Description
UC is a chronic inflammatory bowel disorder with relapsing and remitting course. The incidence of UC in Hong Kong has increased by 30-fold in the past three decades. The efficacy of mesalazine in preventing relapse in patients with UC is well-known and supported by randomized studies. However, mesalazine can be associated with side-effects. In addition, drug compliance is suboptimal, especially when disease is not active. Without mesalazine, the risk of relapse in UC in one year is approximately 60-70%. Repeated flares are disabling for the patient, and lead to increased hospitalisations, anatomical extension of disease, and increased cancer risk. In Hong Kong, 90 percent of patients with UC have low to medium compliance to mesalazine, and 50 percent would prefer the use of a complementary or alternative therapy to maintain disease remission. Identification of a natural product that is effective, acceptable, inexpensive and non-toxic remains an unmet need in patients with UC. Curcumin is a natural phytochemical derived from the Indian spice turmeric. It is widely used, has potent anti-inflammatory, anti-oxidant and anti-tumour properties. Preclinical studies in experimental animals showed that curcumin is effective in preventing colitis. We reported in a randomized study that curcumin is effective in the induction of remission in patients with mild to moderately active UC. Although curcumin is popular amongst patients with inflammatory bowel disease, its efficacy in maintaining disease remission in UC is uncertain. We propose a double-blind, placebo-controlled trial to assess the efficacy of curcumin in preventing clinical relapse in patients with UC. Patients will be randomised to 2 gram curcumin once daily or an equivalent placebo for 12 months. The primary outcome is the rate of clinical relapse at 12 months. Secondary outcomes include adverse events, endoscopic remission, fecal calprotectin levels and time to relapse. Because the use of curcumin is already popular in Asia, this important clinical question will not be a priority of pharmaceutical companies. If proven, this industry-independent trial will be a landmark study that identifies an alternative effective treatment to maintain disease remission in patients with UC. Regardless of the outcome, it will inform clinical practice and provide invaluable data to international guideline committees on the management of this chronic inflammatory disease. The aims of this double-blind, placebo-controlled randomized trial is to assess the efficacy of curcumin in the prevention of relapse in patients with ulcerative colitis (UC).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ulcerative Colitis in Remission

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Masking Description
Double-blinded using identical looking products in both arms
Allocation
Randomized
Enrollment
29 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Curcumin
Arm Type
Active Comparator
Arm Description
Dietary supplements of Curcumin capsules
Arm Title
Curcumin Placebo
Arm Type
Placebo Comparator
Arm Description
Identical looking placebo of the active arm
Intervention Type
Dietary Supplement
Intervention Name(s)
Curcumin
Other Intervention Name(s)
Turmeric
Intervention Description
3g of Curcumin per day
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Curcumin placebo
Intervention Description
3g of Curcumin Placebo per day
Primary Outcome Measure Information:
Title
The relapse rate at 12 months
Description
Defined as clinical symptoms (increased bowel frequency with a bowel frequency Mayo subscore ≥ 1 or rectal bleeding with a Mayo rectal bleeding subscore ≥ 1) together with endoscopic evidence of active disease (Mayo endoscopic subscore ≥ 2).
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Adverse events
Description
The severity grading of AEs will be assessed as Grade 1, 2, 3, 4 or 5 using the Common Terminology Criteria for Adverse Events (CTCAE) Version 4.03 Grading Scale, which can be found at: http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010-06-14_QuickReference_8.5x11.pdf
Time Frame
1 year
Title
Endoscopic remission
Description
Defined as a mayo endoscopic subscore of 0 or 1
Time Frame
1 year
Title
Simple Clinical Colitis Activity Index (SCCAI)
Description
compare the scores in two groups
Time Frame
1 year
Title
Fecal calprotectin levels at 12 months
Description
compare the difference of the levels between groups
Time Frame
1 year
Title
Fecal immunochemical test (FIT) at 12 months
Description
compare the positivity rate in those with flare
Time Frame
1 year
Title
Quality of Life assessed by the Inflammatory Bowel Disease Questionnaire (IBDQ)
Description
compare the scores in two groups
Time Frame
1 year
Title
Patient Reported Outcomes (PRO) Questionnaire
Description
The questionnaire will ask during the study follow up about the psychological aspects of UC patients, the baseline and score on final visit will be compared, as well as between the two groups
Time Frame
1 year
Title
Pharmacokinetics study to measure the drug concentration-time courses
Description
compare the absorption rate in two groups and to establish and evaluate the relationships and subsequently describe the effect-time courses of curcumin absorption in blood and colon.
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: in clinical remission for at least 1 month, defined as Mayo bowel frequency subscore ≤ 1 and Mayo rectal bleeding subscore = 0 (Table 2). a history of at least one flare with symptoms that required intervention within 24 months before screening age ≥ 18 written informed consent obtained Exclusion Criteria: receipt of immunosuppressive drugs or corticosteroids within 60 days of screening prior bowel surgery except appendectomy with severe relapse (Mayo score 9-12) in the last 3 months History or evidence of incompletely resected colonic mucosal dysplasia on regular curcumin supplements or intake of curry in diet for ≥5 days each week presence of infections (exclude simple infections such as influenza, etc.) or sepsis pregnancy or lactating women with a Mayo endoscopic subscore ≥2 on sigmoidoscopy or colonoscopy at baseline allergic to curry-related products
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Siew Ng, Prof.
Organizational Affiliation
Chinese University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Prince of Wales Hospital
City
Hong Kong
ZIP/Postal Code
0000
Country
Hong Kong

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
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23040451
Citation
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Curcumin for Prevention of Relapse in Patients With Ulcerative Colitis

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