Anthocyanin Extract and Phospholipid Curcumin in Colorectal Adenoma (MIRACOL)
Primary Purpose
Colorectal Adenoma, Risk Reduction
Status
Unknown status
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Mirtoselect® + Meriva®
Placebo
Sponsored by
About this trial
This is an interventional prevention trial for Colorectal Adenoma
Eligibility Criteria
Inclusion criteria:
- Subjects with colorectal adenomatous polyps greater than 1 cm in maximum diameter not suitable to immediate complete removal;
- Normal renal and hepatic function;
- WHO Performance status=0;
Exclusion Criteria:
- Presence of hyperplastic polyps and/or flat adenomas;
- Subjects with pre-existing colorectal cancer;
- Presence of carcinomatous tissue in adenoma;
Sites / Locations
- ASL 3, Ospedale Villa Scassi, S.C. Gastroenterologia
- Medical Oncology Ente Ospedaliero Ospedali Galliera
- ASL4 Chiavarese, Ospedale di Lavagna, SSD Gastroenterologia
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Anthocyanins+Phospholipidic Curcumin
placeboA + placeboB
Arm Description
Mirtoselect ® 500 mg tablet, 1000 mg (two oral tablets) per day and Meriva ®, 500 mg tablet, 1000 mg (two oral tablets) per day for 28 days
placeboA + placeboB per day for four weeks
Outcomes
Primary Outcome Measures
Change of immunohistochemical expression of beta catenin in normal and adenomatous colonic tissue
Secondary Outcome Measures
Change of IHC Nuclear Factor-Kβ (NFKβ), Ki-67 Labeling Index and P53 in normal and adenomatous mucosa.
Full Information
NCT ID
NCT01948661
First Posted
January 18, 2013
Last Updated
July 31, 2018
Sponsor
Ente Ospedaliero Ospedali Galliera
Collaborators
Fondazione Umberto Veronesi, Indena S.p.A
1. Study Identification
Unique Protocol Identification Number
NCT01948661
Brief Title
Anthocyanin Extract and Phospholipid Curcumin in Colorectal Adenoma
Acronym
MIRACOL
Official Title
Randomized Window of Opportunity Trial of Anthocyanin Extract and Phospholipid Curcumin in Subjects With Colorectal Adenoma
Study Type
Interventional
2. Study Status
Record Verification Date
July 2018
Overall Recruitment Status
Unknown status
Study Start Date
March 2014 (undefined)
Primary Completion Date
September 2019 (Anticipated)
Study Completion Date
December 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ente Ospedaliero Ospedali Galliera
Collaborators
Fondazione Umberto Veronesi, Indena S.p.A
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Colonic adenomatous polyps are pre cancer lesions and are used as intermediate markers for testing agents with potential cancer prevention.
Meriva© is a bioavailable form of curcumin, a polyphenolic compound obtained from turmeric (Curcuma longa L.) endowed with anti-inflammatory, antioxidant and antitumor effects. In vivo data indicate that curcumin formulated with phosphatidylcholine furnishes higher blood levels of parent agent than natural curcumin.
Mirtoselect©, an anthocyanin mixture from bilberry containing isolated cyanidin-3-glucoside (C3G), the most abundant anthocyanin in diet, prevents intestinal adenoma formation in the Apc(Min) mouse model.
The investigators hypothesize that the combination of both agents will decrease the expression of proteins involved in colon tumorigenesis relative to placebo.
The change of biomarker expression between pre-treatment biopsy and post-treatment endoscopic resection in the target adenoma and the normal rectal mucosa will be the response measures.
The primary response measure is the change of immunohistochemical (IHC) expression of β-catenin in adenomatous tissue and normal rectal mucosa. Secondary response measures are the changes of IHC Nuclear Factor-Kβ (NFKβ), cell proliferation by Ki-67 Labeling Index and apoptosis by P53 in adenomatous and adjacent normal mucosa.
The study design is a phase II, randomized, double blind, placebo controlled, window of opportunity trial of the combination of Mirtoselect 1 gr/day+Meriva 1 gr/day or placebo. Subjects with histological confirmation of colorectal adenomatous polyps >1 cm not suitable to immediate complete removal will be enrolled in a 4-week intervention trial before endoscopic polypectomy.
The demonstration of a biological activity of the two agent combination may provide the rationale for a phase III trial aimed at reducing the risk of colon cancer in high risk subjects.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Adenoma, Risk Reduction
7. Study Design
Primary Purpose
Prevention
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
Anthocyanins+Phospholipidic Curcumin
Arm Type
Experimental
Arm Description
Mirtoselect ® 500 mg tablet, 1000 mg (two oral tablets) per day and Meriva ®, 500 mg tablet, 1000 mg (two oral tablets) per day for 28 days
Arm Title
placeboA + placeboB
Arm Type
Placebo Comparator
Arm Description
placeboA + placeboB per day for four weeks
Intervention Type
Dietary Supplement
Intervention Name(s)
Mirtoselect® + Meriva®
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Primary Outcome Measure Information:
Title
Change of immunohistochemical expression of beta catenin in normal and adenomatous colonic tissue
Time Frame
baseline and 4 weeks
Secondary Outcome Measure Information:
Title
Change of IHC Nuclear Factor-Kβ (NFKβ), Ki-67 Labeling Index and P53 in normal and adenomatous mucosa.
Time Frame
baseline and 4 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria:
Subjects with colorectal adenomatous polyps greater than 1 cm in maximum diameter not suitable to immediate complete removal;
Normal renal and hepatic function;
WHO Performance status=0;
Exclusion Criteria:
Presence of hyperplastic polyps and/or flat adenomas;
Subjects with pre-existing colorectal cancer;
Presence of carcinomatous tissue in adenoma;
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrea DeCensi, MD
Organizational Affiliation
Medical Oncology Ente Ospedaliero Ospedali Galliera
Official's Role
Principal Investigator
Facility Information:
Facility Name
ASL 3, Ospedale Villa Scassi, S.C. Gastroenterologia
City
Genova
ZIP/Postal Code
16100
Country
Italy
Facility Name
Medical Oncology Ente Ospedaliero Ospedali Galliera
City
Genova
ZIP/Postal Code
16128
Country
Italy
Facility Name
ASL4 Chiavarese, Ospedale di Lavagna, SSD Gastroenterologia
City
Lavagna
ZIP/Postal Code
16033
Country
Italy
12. IPD Sharing Statement
Learn more about this trial
Anthocyanin Extract and Phospholipid Curcumin in Colorectal Adenoma
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