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Clinical Trials/NCT03625089
NCT03625089
Withdrawn
N/A

The Impact of Nurse-led Programme With and Without Carotid Ultrasound on Addressing Cardiovascular Risk in Patients With Arthritis: a Prospective, Multicentre, Randomised, Controlled Trial

Chinese University of Hong Kong1 site in 1 countrySeptember 1, 2018

Overview

Phase
N/A
Intervention
Atorvastatin
Conditions
Arthritis, Rheumatoid
Sponsor
Chinese University of Hong Kong
Locations
1
Primary Endpoint
change in Framingham risk score
Status
Withdrawn
Last Updated
6 years ago

Overview

Brief Summary

Elevated CVD risk is a significant public health problem that contributes greatly to the increased morbidity and shortened lifespan of individuals with RA and PsA. Over the past decades, there has been great progress into the understanding of the severity of CVD risk in these patients but these risk factors are not well managed. The development of the high-risk strategy is therefore necessary, with more intensive therapy reserved for patients identified as high-risk, e.g. because they have high-risk FRS. However, these risk scores under-estimated CV risk in patients with RA and PsA. An intermediate approach is to use quantification of preclinical vascular disease to further identify high-risk patients. Results from this study will provide clinical implications in terms of detecting and managing cardiovascular morbidity in patients with RA and PsA.

Detailed Description

Objectives This study investigates the impact of a nurse-led programme on cardiovascular (CV) risk screening with and without carotid ultrasound for carotid plaque on CV risk factor control in asymptomatic rheumatoid arthritis (RA) and psoriatic arthritis (PsA) patients. Hypothesis The investigators hypothesize that CV risk stratification and management in RA and PsA may be improved by incorporation of carotid ultrasound to assess for carotid plaque.

Registry
clinicaltrials.gov
Start Date
September 1, 2018
End Date
September 30, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Lai-Shan Tam

Professor

Chinese University of Hong Kong

Eligibility Criteria

Inclusion Criteria

  • Patients with RA fulfilled the 2010 ACR/EULAR classification criteria or PsA fulfilled the Classification of Psoriatic Arthritis (CASPAR) criteria
  • aged between 18 and 75 will be recruited.

Exclusion Criteria

  • had a history of overt CVD (ie, symptomatic coronary artery disease \[CAD\] or ischemic stroke or transient ischemic attack or peripheral vascular disease)
  • had significant co-morbidities including severe renal impairment or severe deranged liver function
  • female of childbearing potential who are unwilling to use adequate contraception, pregnant or breastfeeding women
  • patients who are already taking lipid lowering therapy.

Arms & Interventions

Group 1 - FRS arm

Both group will participate in the nurse-led programme on CV risk screening and carotid ultrasound for carotid plaque assessment. Subjects in group 1 will initiate Atorvastatin treatment (20mg daily per oral) if their Framingham Risk Score \>10%

Intervention: Atorvastatin

Group 2 USG arm

Subjects in group 2 will initiate Atorvastatin treatment (20mg daily per oral) if they had carotid plaque upon carotid ultrasound findings..

Intervention: Atorvastatin

Outcomes

Primary Outcomes

change in Framingham risk score

Time Frame: 12 months

The Framingham Risk Score is a gender-specific algorithm used to estimate the 10-year cardiovascular risk of an individual. Individuals with low risk have 10% or less CHD risk at 10 years, with intermediate risk 10-20%, and with high risk 20% or more. Change in Framingham risk score between subject in two group will be evaluated. A positive change in score indicates increased CV risk, vice versa.

Secondary Outcomes

  • Change in pulse wave velocity (PWV) in subjects(12 months)
  • Change in augmentation index (AIX) in subjects(12 months)
  • The number of measures taken against comorbidities(12 months)
  • Changes in intima-media thickness (IMT)(12 months)
  • Proportions of patients achieving remission(12 months)
  • Change in individual modifiable risk factors levels(12 months)
  • Proportion of plaque progression(12 months)

Study Sites (1)

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