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Effect van broccoli zaailingen op ontsteking en insuline gevoeligheid na een testmaaltijd.

Effect of broccoli seedlings on postprandial inflammation and insulin sensitivity.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON20949
Enrollment
12
Registered
2012-05-16
Start date
2012-06-18
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

insulin resistance, inflammation

Interventions

Intervention with broccoli seedlings (BroccoCress). Butter letuce will be used as a control. Volunteers received 75 gram glucose in 250 mL tap water, leading to postprandial inflammation as measured

Sponsors

University Medical Center Groningen
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Healthy male volunteer aged 18 to 30 and BMI 18-25 kg/m2, extremities included; 2. Not involved in intensive sportive activities more than twice a week (e.g. playing football, tennis, running, race-cycling, swimming); 3. Stable weight and no intention to lose weight until completion of the study; 4. Signed written informed consent form (ICF).

Exclusion criteria

Exclusion criteria: 1. Not being able to fast overnight (10 hours); 2. Vegetarians; 3. Documented Diabetes mellitus or fasting glucose level of >6.1mmol/l at screening; 4. Clinically significant inflammatory disease (possibly interfering with measurement of parameters in this study); 5. Intake of medication (from 2 weeks before screening until the end of the study, except for sporadic use of paracetamol and/or treating an AE); 6. Smoking; 7. Donation of blood within the last 3 months prior to admission to the clinic; 8. Participation to another clinical study within 90 days before enrolment; 9. Positive drug screen or alcohol breath test at D-1; 10. Fear of blood and/or needles; 11. Veins unsuitable for intravenous (i.v.) catheter on either arm (e.g., veins that are difficult to locate, access or puncture, veins with a tendency to rupture during or after puncture); 12. Clinically relevant abnormalities in clinical chemistry, hemoglobin or positive HIV, HbsAg and/or HepC at screening.

Design outcomes

Primary

MeasureTime frame
The main outcomes of this study are inflammation and insulin sensitivity. Inflammation will be addressed by PBMC activation as measured by nuclear translocation of NF-kappaB, plasma cytokine levels and insulin sensitivity as determined by plasma concentrations of glucose and insulin as well as the uptake of glucose in tissues.

Secondary

MeasureTime frame
Sulforaphane kinetics, measured in plasma and urine.

Contacts

Public ContactM.G. Priebe

University Medical Center Groningen (UMCG) Antonius Deusinglaan 1

m.g.priebe@med.umcg.nl+31 (0)50 3619386

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)