The Impact of Artichoke Leaf Extract on Blood Cholesterol: Primary Study
Primary Purpose
Lipid Metabolism Disorders
Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Artichoke Leaf Extract
Placebo
Sponsored by
About this trial
This is an interventional supportive care trial for Lipid Metabolism Disorders focused on measuring Lipids, Cholesterol, Dietary Supplements, Cynara scolymus, Safety
Eligibility Criteria
Inclusion Criteria:
- ≥18 years of age
- HDL cholesterol <40 mg/dL in men or <50 mg/dL in women
- BMI ≥25 kg/m2.
Exclusion Criteria:
- Patient on statins
- Triglycerides >400 mg/dL
- Low density lipoprotein (LDL) >190 mg/dL
- Significant hepatic disease (i.e., documented diagnosis of hepatic cancer, hepatitis, or cirrhosis)
- Significant renal disease (i.e., most recent glomerular filtration rate <30 mL/min/1.73 m2)
- Significant gastrointestinal tract disease (documented diagnosis of malabsorption disorder, GI cancer, or uncontrolled inflammatory bowel disease)
- History of transplant
- Women of reproductive potential not receiving birth control
- Pregnant/nursing women
Sites / Locations
- University of Mississippi Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Artichoke Leaf Extract
Placebo
Arm Description
Pycrinil® 100 mg/flaxseed oil 380 mg liquid filled hard plant based capsules (Licaps®) twice daily with food
Placebo/flaxseed oil 380 mg liquid filled hard plant based capsules (Licaps®) twice daily with food
Outcomes
Primary Outcome Measures
Change in Concentrations of High Density Lipoprotein Cholesterol
Secondary Outcome Measures
Full Information
NCT ID
NCT02270164
First Posted
October 9, 2014
Last Updated
May 18, 2016
Sponsor
University of Mississippi Medical Center
Collaborators
Indena S.p.A
1. Study Identification
Unique Protocol Identification Number
NCT02270164
Brief Title
The Impact of Artichoke Leaf Extract on Blood Cholesterol: Primary Study
Official Title
The Impact of Artichoke Leaf Extract on Blood Cholesterol: Primary Study
Study Type
Interventional
2. Study Status
Record Verification Date
May 2016
Overall Recruitment Status
Withdrawn
Why Stopped
Sponsor discontinued funding due to higher than anticipated manufacturer costs
Study Start Date
October 2014 (undefined)
Primary Completion Date
February 2016 (Actual)
Study Completion Date
February 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Mississippi Medical Center
Collaborators
Indena S.p.A
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Pycrinil® is a purified extract of the artichoke leaf. Artichoke leaf extract (ALE) has some clinical trial data suggesting benefit in the treatment of cholesterol disorders in several countries, but this effect has not been studied in a U.S. population. The investigators will give ALE or a placebo to overweight men and women with low "good" cholesterol to see if ALE increases their good cholesterol. The investigators will also make sure that ALE is safe.
Detailed Description
Subjects will be divided into one of two groups: (1) Pycrinil®/flaxseed oil or (2) Placebo/flaxseed oil twice daily with food. The two formulations will be identical in appearance and standardized by Indena, S.p.A. Patients will be enrolled for a total of 3 months (± 1 week to allow for scheduling flexibility) with a 1 month (± 1 week to allow for scheduling flexibility) first follow-up visit in between enrollment and final visits. At all visits, patients will be asked to monitor for any symptomatic ADE. The first follow-up visit will focus on medication compliance (via pill count) and safety assessment (including laboratories). The final study visit will consist of brief clinical assessment (including anthropometrics), completed lifestyle and physical activity assessments, subjective ADE reporting, and donated blood and urine for clinical laboratory tests. Medication changes are not prohibited during the study period, but must be recorded. Medication bottles will be collected at the first follow-up and final visits; pill counts will be performed to assess compliance.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lipid Metabolism Disorders
Keywords
Lipids, Cholesterol, Dietary Supplements, Cynara scolymus, Safety
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Artichoke Leaf Extract
Arm Type
Experimental
Arm Description
Pycrinil® 100 mg/flaxseed oil 380 mg liquid filled hard plant based capsules (Licaps®) twice daily with food
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo/flaxseed oil 380 mg liquid filled hard plant based capsules (Licaps®) twice daily with food
Intervention Type
Dietary Supplement
Intervention Name(s)
Artichoke Leaf Extract
Other Intervention Name(s)
Pycrinil
Intervention Description
Capsule
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Capsule
Primary Outcome Measure Information:
Title
Change in Concentrations of High Density Lipoprotein Cholesterol
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
≥18 years of age
HDL cholesterol <40 mg/dL in men or <50 mg/dL in women
BMI ≥25 kg/m2.
Exclusion Criteria:
Patient on statins
Triglycerides >400 mg/dL
Low density lipoprotein (LDL) >190 mg/dL
Significant hepatic disease (i.e., documented diagnosis of hepatic cancer, hepatitis, or cirrhosis)
Significant renal disease (i.e., most recent glomerular filtration rate <30 mL/min/1.73 m2)
Significant gastrointestinal tract disease (documented diagnosis of malabsorption disorder, GI cancer, or uncontrolled inflammatory bowel disease)
History of transplant
Women of reproductive potential not receiving birth control
Pregnant/nursing women
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniel M Riche, PharmD
Organizational Affiliation
University of Mississippi Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Mississippi Medical Center
City
Jackson
State/Province
Mississippi
ZIP/Postal Code
39216
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
18424099
Citation
Bundy R, Walker AF, Middleton RW, Wallis C, Simpson HC. Artichoke leaf extract (Cynara scolymus) reduces plasma cholesterol in otherwise healthy hypercholesterolemic adults: a randomized, double blind placebo controlled trial. Phytomedicine. 2008 Sep;15(9):668-75. doi: 10.1016/j.phymed.2008.03.001.
Results Reference
background
PubMed Identifier
10758778
Citation
Englisch W, Beckers C, Unkauf M, Ruepp M, Zinserling V. Efficacy of Artichoke dry extract in patients with hyperlipoproteinemia. Arzneimittelforschung. 2000 Mar;50(3):260-5. doi: 10.1055/s-0031-1300196.
Results Reference
background
PubMed Identifier
22746542
Citation
Rondanelli M, Giacosa A, Opizzi A, Faliva MA, Sala P, Perna S, Riva A, Morazzoni P, Bombardelli E. Beneficial effects of artichoke leaf extract supplementation on increasing HDL-cholesterol in subjects with primary mild hypercholesterolaemia: a double-blind, randomized, placebo-controlled trial. Int J Food Sci Nutr. 2013 Feb;64(1):7-15. doi: 10.3109/09637486.2012.700920. Epub 2012 Jun 29.
Results Reference
background
PubMed Identifier
23543518
Citation
Wider B, Pittler MH, Thompson-Coon J, Ernst E. Artichoke leaf extract for treating hypercholesterolaemia. Cochrane Database Syst Rev. 2013 Mar 28;(3):CD003335. doi: 10.1002/14651858.CD003335.pub3.
Results Reference
background
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The Impact of Artichoke Leaf Extract on Blood Cholesterol: Primary Study
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