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Investigations on the Effect of Kale on the Lipid Status

Investigations on the Effect of Kale on the Lipid Status (Untersuchungen Zum Einfluss Von Grünkohl Auf Den Lipidstatus)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03545555
Acronym
HypocholKale
Enrollment
40
Registered
2018-06-04
Start date
2018-04-13
Completion date
2020-12-31
Last updated
2018-06-04

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

Conditions

Effects of Kale Ingredients on Lipid Status Parameter

Keywords

kale, antioxidant capacity, cholesterol, lipid status

Brief summary

This intervention study investigates the effects of various kale preparations (dietary supplements) on lipid status parameters. Within the study period of 8 weeks, three blood withdrawals are planned (week 0, 4 and 8) for the volunteers. Lipid status parameters (total cholesterol, HDL cholesterol, LDL cholesterol, triacylglycerides) will be determined in blood. There is a correlation between contents of LDL cholesterol, total cholesterol and triacylglycerides and the risk for cardiovascular diseases (CVD). In contrast, a high content of HDL cholesterol is correlated with a lower risk for CVD. In addition, the contents of apolipoprotein A1 and apolipoprotein B will be analysed.

Interventions

DIETARY_SUPPLEMENTKale Preparation Kale Powder

Effect of kale preparation kale powder on lipid status

DIETARY_SUPPLEMENTKale Preparation Kale Extract

Effect of kale preparation kale extract on lipid status

DIETARY_SUPPLEMENTKale Preparation Flavonoid Extract

Effect of kale preparation flavonoid extract on lipid status

DIETARY_SUPPLEMENTPlacebo

Effect of placebo on lipid status

Sponsors

University of Jena
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* total cholesterol \> 200 mg/dl

Exclusion criteria

* LDL cholesterol \< 130 mg/dl * medication to lower blood lipids * genetically based hypercholesterolemia

Design outcomes

Primary

MeasureTime frameDescription
Change of lipid status parametersweeks 0, 4 and 8total cholesterol, HDL cholesterol, LDL cholesterol

Secondary

MeasureTime frameDescription
Change of apolipoproteinsweeks 0, 4 and 8apolipoprotein A1 and apolipoprotein B
Change of antioxidant capacityweeks 0, 4 and 8lipophilic antioxidant capacity (L-TEAC)

Countries

Germany

Contacts

Primary ContactVolker Böhm, PD Dr.
Volker.Boehm@uni-jena.de+49-(0)3641-9496

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026