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postprandial Lipidmetabolism in hMe subjects and healthy controls

postprandial Lipidmetabolism in hMe subjects and healthy controls - LIME study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON37127
Enrollment
30
Registered
2012-12-12
Start date
2013-01-10
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

postprandial dyslipidimia postprandial lipidmetabolism disorder

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Male and female subjects at least 18 years of age Clinically esthablished diagnosis of HME or unaffected, healthy control willing to stop ATII/ACE inhibitors (5 days) and statin (4 weeks) before lipidload

Exclusion criteria

Exclusion criteria: Current diabetes Current pregnancy Malignancy with limited lifespan -Cardiovascular disease

Design outcomes

Primary

MeasureTime frame
Changes in postprandial trygliceride levels in HME subjects vewith either EXT1 or EXT2 mutation compared to unaffected, healthy control subjects

Secondary

MeasureTime frame
Changes in cardiovascular risk profile (lipidprofile, ECG changes) in HME subjects vewith either EXT1 or EXT2 mutation compared to unaffected, healthy control subjects

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)