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Tracking of Lipid Lowering Therapy in Jordan (JoLLA)

J

Jordan Collaborating Cardiology Group

Status

Terminated

Conditions

Atherosclerotic Cardiovascular Disease
Dyslipidemias

Study type

Observational

Funder types

Other

Identifiers

NCT05629767
JCCG.JoLLA.10.2022

Details and patient eligibility

About

The present study aims to examine the clinical practice of modifying the dose of lipid-lowering therapy in patients with atherosclerotic cardiovascular disease (ASCVD), who have LDL-C > 70 mg/dl despite statin treatment.

Full description

ASCVD is the leading cause of morbidity and mortality worldwide, in the Middle East and in Jordan. One of the major risk factors that contribute to the development and progression of ASCAD is dyslipidemia. A large number of clinical trials have reported the benefits of lowering LDL-C, in reducing the mortality rate among ASCAD patients.

The 2019 ACC/AHA blood cholesterol treatment guideline to reduce atherosclerotic cardiovascular risk in adults has expanded the role of LDL-C targets and reiterated the importance of achieving an LDL-C level of 70 mg/dl or less for patients who have ASCVD.

Patients on statins and other lipid-lowering therapy in Jordan have not been tracked in the past for the potential of up escalating the lipid-lowering therapy to reach the LDL-C target.

The investigation will enroll patients with ASCVD who have LAL-C >70 mg/dl on lipid-lowering therapy and follow them for 12 months to examine the treating physicians' action in up-titrating the lipid-lowering therapy dose(s) and the frequency of measuring serum lipids during the study period.

Enrollment

1,000 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria

  1. Adults aged 18 years or old.
  2. Presence of atherosclerotic cardiovascular disease on lipid-lowering therapy.
  3. LDL-C > 70mg/dl.
  4. Willingness to sign an informed consent.

Exclusion criteria

  1. Life-threatening disease with limited survival.
  2. Unwillingness to sign an informed consent.

Trial design

1,000 participants in 1 patient group

Patients with ASCVD
Description:
Patients with ASCVD on statins and LDL-C more than 70 mg/dl

Trial documents
1

Trial contacts and locations

2

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Central trial contact

Wesam Al Saud, PharmD; Ayman Hammoudeh, MD FACC

Data sourced from clinicaltrials.gov

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