Last reviewed · How we verify

NCT01280604

Effects of Fenofibrate 160mg to 54mg Conversion on Triglyceride Levels in Patients on Statin Therapy

Completed NA Results posted Last updated 4 June 2015
What this trial tests

NA trial testing Fenofibrate 54mg in Hyperlipidemias in 66 participants. Completed in 1 January 2013.

Timeline
1 October 2010
Primary endpoint
1 January 2013
1 January 2013

Quick facts

Lead sponsorKaiser Permanente
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment66
Start date1 October 2010
Primary completion1 January 2013
Estimated completion1 January 2013
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Kaiser Permanente — full company profile →

Who can join

18 and older, any sex, with Hyperlipidemias. Healthy volunteers can join.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The primary objective of this randomized trial is to measure the impact of converting patients on statin therapy from fenofibrate 160mg to 54mg per day compared to patients who continue fenofibrate 160mg per day for triglycerides.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Hyperlipidemias

Currently open trials in the same condition.

Other Kaiser Permanente trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01280604.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing