NCT Number: NCT00485095
The Effect of Plant Sterol Supplement on Blood Cholesterol
The purpose of this study is to determine whether supplement of plant sterol could lower blood cholesterol.
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Notify MeKey information
Conditions
Age range
18 year–80 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 4
Primary location
Lipidklinikken, Rikshospitalet Radiumhospitalet HF, Oslo, Norway
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Men and women 18-80 years old
- Total cholesterol: 4.5-7.5 mmol/l
- Triglycerides at or below 4.0 mmol/l
Exclusion criteria
- BMI at or above 35 kg/m2
- Secondary hyperlipidemia, included diabetes
- Hypertension (at og higher than 170/110)
- Coronar, perifery or cerebral vascular disease last 3 months
- Familial hypercholesterolemia
- Change in dose of statins, oestrogen or contraceptives last 3 months
- Taking drugs which are known to interfere with the plasma level of cholesterol
- Chronic rheumatoid diseases or other diseases known to affect c-reactive protein
- Pregnancy
- Lactation
- Planning to reduce weight
- Taking plant sterols
Treatment and study plan
Sponsors and collaborators
Lead sponsor
Oslo University Hospital
Other
Collaborators
- Mills DA
Registry information
Official study title
A Single Centre, Randomized Crossover Double-Blind Placebo-Controlled Study to Measure the Effect of Plant Sterol Supplement on Blood Cholesterol
Important dates
- Study start
- 2007
- Primary completion
- 2007
- Study completion
- 2007
- First posted
- Jun 12, 2007
- Registry last updated
- Jul 1, 2011
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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