Omega 3 Fatty Acids in Colorectal Cancer (CRC) Prevention in Patients With Lynch Syndrome (COLYNE)
Primary Purpose
Colorectal Cancer, Lynch Syndrome
Status
Active
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Omega-3 fatty acid ethyl esters (2 gram)
Sponsored by
About this trial
This is an interventional treatment trial for Colorectal Cancer focused on measuring Omega 3
Eligibility Criteria
Inclusion Criteria:
- Ability of participant or Legally Authorized Representative (LAR) to understand this study, and participant or LAR willingness to sign a written informed consent
- Candidate for elective endoscopy procedure
- Participants with known Lynch Syndrome
- Eastern Cooperative Oncology Group (ECOG) Performance Status 0-1
- Willing to undergo a colonoscopy and biopsy at baseline and another colonoscopy and biopsy at 12 months visit.
- Participants taking Aspirin for chemoprevention must agree to stop it for at least 4 weeks prior to study entry and throughout the trial period
- Adequate organ and marrow function
- Women of child-bearing potential and men with partners of child-bearing potential must agree to practice sexual abstinence, or to use two forms of adequate contraception (hormonal AND barrier method of birth control) prior to study entry, for the duration of study participation, and for 90 days following completion of therapy. If a woman becomes pregnant or suspects she is pregnant while participating in this study, she should inform her treating physician immediately.
- Men of child-bearing potential must not father a child or donate sperm while on this study and for 90 days after their last study treatment.
Exclusion Criteria:
- Current or anticipated use of other investigational agents while participating in this study.
- Psychiatric illness/social situations that could limit compliance with study requirements.
- Pregnant or breast feeding.
- Familial adenomatous polyposis, Putz-Jeghers disease, ulcerative colitis, or Crohn's disease.
- Previous or known active malignancies, except non-melanoma skin cancers, unless curatively treated and with no evidence of recurrence for more than 5 years
- Current use of anticoagulation therapy
- Current use of therapeutic doses of aspirin for reasons other than chemoprevention
- Use of omega 3 fatty acids or flaxseed supplements within 4 weeks before this study's screening/baseline colonoscopy
- Use of high dose omega 3 fatty acids within the past 3 months prior to study baseline/screening
- Current, regular use of non-steroidal anti-inflammatory drugs (NSAIDS)
- Allergy to fish and/or fish products
- Uncontrolled infectious disease
- Malabsorption syndrome, disease affecting gastrointestinal function, or previous resection of the stomach or small bowel.
- Unable to swallow and retain oral medication
Sites / Locations
- The University of Kansas Cancer Center, Westwood Campus
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Omega-3, 2 grams
Arm Description
Omega-3 fatty acid ethyl esters (2 grams) orally (by mouth) once per day for 12 months
Outcomes
Primary Outcome Measures
Retention rate of participants
Feasibility is defined as at least 80% retention rate
Secondary Outcome Measures
Proportion of participants with treatment-related adverse events in each arm.
Measured by Common Terminology Criteria Adverse Events (CTCAE) V5.0
Full Information
NCT ID
NCT03831698
First Posted
February 4, 2019
Last Updated
May 31, 2023
Sponsor
University of Kansas Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT03831698
Brief Title
Omega 3 Fatty Acids in Colorectal Cancer (CRC) Prevention in Patients With Lynch Syndrome (COLYNE)
Official Title
Omega 3 Fatty Acids in Colorectal Cancer (CRC) Prevention in Patients With Lynch Syndrome (COLYNE)
Study Type
Interventional
2. Study Status
Record Verification Date
May 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
February 6, 2019 (Actual)
Primary Completion Date
June 8, 2022 (Actual)
Study Completion Date
August 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Kansas Medical Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This is a pilot study aimed at assessing the effects of moderate dose omega-3-acid ethyl esters capsules (generic Lovaza) on molecular, and intestinal microbiota changes in participants at high risk for colorectal cancer. The study will be a single arm, open label study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer, Lynch Syndrome
Keywords
Omega 3
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
21 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Omega-3, 2 grams
Arm Type
Experimental
Arm Description
Omega-3 fatty acid ethyl esters (2 grams) orally (by mouth) once per day for 12 months
Intervention Type
Drug
Intervention Name(s)
Omega-3 fatty acid ethyl esters (2 gram)
Other Intervention Name(s)
lovaza
Intervention Description
Omega-3 fatty acid ethyl esters (2 gram)
Primary Outcome Measure Information:
Title
Retention rate of participants
Description
Feasibility is defined as at least 80% retention rate
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Proportion of participants with treatment-related adverse events in each arm.
Description
Measured by Common Terminology Criteria Adverse Events (CTCAE) V5.0
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Ability of participant or Legally Authorized Representative (LAR) to understand this study, and participant or LAR willingness to sign a written informed consent
Candidate for elective endoscopy procedure
Participants with known Lynch Syndrome
Eastern Cooperative Oncology Group (ECOG) Performance Status 0-1
Willing to undergo a colonoscopy and biopsy at baseline and another colonoscopy and biopsy at 12 months visit.
Participants taking Aspirin for chemoprevention must agree to stop it for at least 4 weeks prior to study entry and throughout the trial period
Adequate organ and marrow function
Women of child-bearing potential and men with partners of child-bearing potential must agree to practice sexual abstinence, or to use two forms of adequate contraception (hormonal AND barrier method of birth control) prior to study entry, for the duration of study participation, and for 90 days following completion of therapy. If a woman becomes pregnant or suspects she is pregnant while participating in this study, she should inform her treating physician immediately.
Men of child-bearing potential must not father a child or donate sperm while on this study and for 90 days after their last study treatment.
Exclusion Criteria:
Current or anticipated use of other investigational agents while participating in this study.
Psychiatric illness/social situations that could limit compliance with study requirements.
Pregnant or breast feeding.
Familial adenomatous polyposis, Putz-Jeghers disease, ulcerative colitis, or Crohn's disease.
Previous or known active malignancies, except non-melanoma skin cancers, unless curatively treated and with no evidence of recurrence for more than 5 years
Current use of anticoagulation therapy
Current use of therapeutic doses of aspirin for reasons other than chemoprevention
Use of omega 3 fatty acids or flaxseed supplements within 4 weeks before this study's screening/baseline colonoscopy
Use of high dose omega 3 fatty acids within the past 3 months prior to study baseline/screening
Current, regular use of non-steroidal anti-inflammatory drugs (NSAIDS)
Allergy to fish and/or fish products
Uncontrolled infectious disease
Malabsorption syndrome, disease affecting gastrointestinal function, or previous resection of the stomach or small bowel.
Unable to swallow and retain oral medication
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anwaar Saeed, MD
Organizational Affiliation
The University of Kansas Cancer Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
The University of Kansas Cancer Center, Westwood Campus
City
Kansas City
State/Province
Kansas
ZIP/Postal Code
66205
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Omega 3 Fatty Acids in Colorectal Cancer (CRC) Prevention in Patients With Lynch Syndrome (COLYNE)
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