NCT04220164

Brief Summary

Taipei MacKay Memorial Hospital will establish a Lipid Clinic for hyperlipidemic patients. In this Lipid Clinic, the physician will discuss with each individual patient and set an individualized LDL goal according to current guideline and regulation of National Health Insurance Administration (NHIA). The aim of this study is to observe blood lipid outcomes in patients who receive treatment in Lipid Clinic of Taipei MacKay Memorial Hospital.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
500

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2020

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 26, 2019

Completed
8 days until next milestone

Study Start

First participant enrolled

January 3, 2020

Completed
4 days until next milestone

First Posted

Study publicly available on registry

January 7, 2020

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2020

Completed
5 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2025

Completed
Last Updated

January 7, 2020

Status Verified

January 1, 2020

Enrollment Period

12 months

First QC Date

December 26, 2019

Last Update Submit

January 3, 2020

Conditions

Outcome Measures

Primary Outcomes (1)

  • Lipid profile

    check serum level of LDL-C

    12 month

Study Arms (1)

Dyslipidemic patients

Patients who meet the criteria of high-risk category according to 2017 Taiwan Lipid Guideline for High-Risk Patients have a abnormal serum LDL-C level

Other: Education and inform the optimal threshold of LDL-C levels

Interventions

Physicians educate patients and provide a clear information about optimal LDL-C value according to individual patient's condition according to current guidelines

Dyslipidemic patients

Eligibility Criteria

Age20 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients who are ≥20 years, have abnormal lipid profiles, need lipid-lowering drugs according to 2017 Taiwan Lipid Guideline in Lipid Clinic of Taipei MacKay Memorial Hospital.

You may qualify if:

  • ≥20 years-old
  • Abnormal lipid profiles according to 2017 Taiwan Lipid Guideline for High-risk Patients

You may not qualify if:

  • Reject to participate in this study
  • Pregnant women
  • Prisoner
  • Illiteracy
  • HIV patients
  • Individuals who are mentally retarded, homeless, and handicapped

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Taiwan, Taipei, Mackay Memorial hospital

Taipei, 104, Taiwan

RECRUITING

Related Publications (1)

  • Li YH, Ueng KC, Jeng JS, Charng MJ, Lin TH, Chien KL, Wang CY, Chao TH, Liu PY, Su CH, Chien SC, Liou CW, Tang SC, Lee CC, Yu TY, Chen JW, Wu CC, Yeh HI; Writing Group of 2017 Taiwan Lipid Guidelines for High Risk Patients. 2017 Taiwan lipid guidelines for high risk patients. J Formos Med Assoc. 2017 Apr;116(4):217-248. doi: 10.1016/j.jfma.2016.11.013. Epub 2017 Feb 24.

    PMID: 28242176BACKGROUND

MeSH Terms

Conditions

Dyslipidemias

Interventions

Educational Status

Condition Hierarchy (Ancestors)

Lipid Metabolism DisordersMetabolic DiseasesNutritional and Metabolic Diseases

Intervention Hierarchy (Ancestors)

Socioeconomic FactorsPopulation Characteristics

Study Officials

  • Chao-Feng Lin, PhD

    Mackay Memorial Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Chao-Feng Lin, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
OTHER
Target Duration
5 Years
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 26, 2019

First Posted

January 7, 2020

Study Start

January 3, 2020

Primary Completion

December 31, 2020

Study Completion

December 31, 2025

Last Updated

January 7, 2020

Record last verified: 2020-01

Data Sharing

IPD Sharing
Will not share

We will not provide IPD to other researchers according to IRB regulation.

Locations