Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
18 participants
INTERVENTIONAL
2006-10-31
2007-10-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Flaxseed Mucilage and Satiety
NCT01238744
The Effects of Flaxseed Supplement on Weight and Biochemical Factors in Overweight and Obese Subject
NCT02410668
Effects of Flaxseed Supplementation in Metabolic Syndrome
NCT02497352
The Effects of Flaxseed Supplement on Biochemical Factors and Hepatic Fibrosis in Patients With Nonalcoholic Fatty Liver Disease
NCT02395900
Biomarkers in Post-Menopausal Women Receiving Flaxseed
NCT01698294
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
CROSSOVER
PREVENTION
DOUBLE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Whole flaxseeds, flaxseed mucilage, glucomannan
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Normal weight or moderately overweigh (BMI 25-30 kg/m2)
Exclusion Criteria
* Hemoglobin concentration \<8mmol/L
* Chronic diseases (i.e. diabetes, CVD), hypertension, hyperlipidemia
* Consumption of dietary supplements including vitamin tablets
* Smoking
* Excess physical activity (\>10h of intense physical activity per week)
* Medicine use (not including occasional consumption of pain killers)
18 Years
40 Years
MALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Copenhagen
OTHER
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Søren Toubro, MD
Role: PRINCIPAL_INVESTIGATOR
Institute of Human Nutrition
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Institute of Human Nutrition
Frederiksberg C, , Denmark
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
B226
Identifier Type: -
Identifier Source: secondary_id
KF 01 309595
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.