Canadians Achieve Cholesterol Targets Fast With Atorvastatin Stratified Titration

NCT ID: NCT00150371

Last Updated: 2021-02-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

1100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2004-06-30

Study Completion Date

2005-05-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The objective of this study is to assess the effectiveness of an atorvastatin treatment regimen involving starting doses between 10 and 80 mg, followed by a single-step titration (except for subjects started at 80mg), if required

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Hypercholesterolemia

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

atorvastatin

Intervention Type DRUG

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Age 30 to 79 years old
* Triglyceride level 6.8 mmol/L at screening
* LDL-C of 5.7 mmol/L at screening

Exclusion Criteria

* Pregnant or lactating women, or women of childbearing potential not using an acceptable method of contraception. The latter are defined as: abstinence, surgical sterilization, oral contraceptives for at least 3 cycles, intrauterine device, implant, depot injection, or barrier method in conjunction with contraceptive foam or jelly.
* Subjects whose blood cholesterol levels are controlled (LDL-C targets) with statins other than atorvastatin
* Subjects receiving statin doses higher than the following: 10-40mg for simvastatin , 20-40mg for fluvastatin, pravastatin and lovastatin and 10-20 mg for rosuvastatin. Subjects already treated with atorvastatin at the time of screening are not eligible unless atorvastatin has been discontinued at least 2 months prior to screening
* Subjects receiving 2 or more lipid lowering agents are excluded (statins + resins or fibrates or niacin or fish oils)
Minimum Eligible Age

30 Years

Maximum Eligible Age

79 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Pfizer's Upjohn has merged with Mylan to form Viatris Inc.

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Pfizer CT.gov Call Center

Role: STUDY_DIRECTOR

Pfizer

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Pfizer Investigational Site

Calgary, Alberta, Canada

Site Status

Pfizer Investigational Site

Calgary, Alberta, Canada

Site Status

Pfizer Investigational Site

Calgary, Alberta, Canada

Site Status

Pfizer Investigational Site

Edmonton, Alberta, Canada

Site Status

Pfizer Investigational Site

Edmonton, Alberta, Canada

Site Status

Pfizer Investigational Site

Edmonton, Alberta, Canada

Site Status

Pfizer Investigational Site

Coquitlam, British Columbia, Canada

Site Status

Pfizer Investigational Site

Coquitlam, British Columbia, Canada

Site Status

Pfizer Investigational Site

Kelowna, British Columbia, Canada

Site Status

Pfizer Investigational Site

Langley, British Columbia, Canada

Site Status

Pfizer Investigational Site

Surrey, British Columbia, Canada

Site Status

Pfizer Investigational Site

Vancouver, British Columbia, Canada

Site Status

Pfizer Investigational Site

Victoria, British Columbia, Canada

Site Status

Pfizer Investigational Site

Winnipeg, Manitoba, Canada

Site Status

Pfizer Investigational Site

Winnipeg, Manitoba, Canada

Site Status

Pfizer Investigational Site

Moncton, New Brunswick, Canada

Site Status

Pfizer Investigational Site

Rothesay, New Brunswick, Canada

Site Status

Pfizer Investigational Site

Saint John, New Brunswick, Canada

Site Status

Pfizer Investigational Site

Halifax, Nova Scotia, Canada

Site Status

Pfizer Investigational Site

Halifax, Nova Scotia, Canada

Site Status

Pfizer Investigational Site

Halifax, Nova Scotia, Canada

Site Status

Pfizer Investigational Site

Halifax, B3K 5R3, Nova Scotia, Canada

Site Status

Pfizer Investigational Site

Brampton, Ontario, Canada

Site Status

Pfizer Investigational Site

Burlington, Ontario, Canada

Site Status

Pfizer Investigational Site

Courtice, Ontario, Canada

Site Status

Pfizer Investigational Site

Downsview, Ontario, Canada

Site Status

Pfizer Investigational Site

Fort Erie, Ontario, Canada

Site Status

Pfizer Investigational Site

Hamilton, Ontario, Canada

Site Status

Pfizer Investigational Site

Hawkesbury, Ontario, Canada

Site Status

Pfizer Investigational Site

Kitchener, Ontario, Canada

Site Status

Pfizer Investigational Site

Lindsay, Ontario, Canada

Site Status

Pfizer Investigational Site

Markham, Ontario, Canada

Site Status

Pfizer Investigational Site

Midland, Ontario, Canada

Site Status

Pfizer Investigational Site

Napanee, Ontario, Canada

Site Status

Pfizer Investigational Site

Newmarket, Ontario, Canada

Site Status

Pfizer Investigational Site

Niagara Falls, Ontario, Canada

Site Status

Pfizer Investigational Site

North Bay, Ontario, Canada

Site Status

Pfizer Investigational Site

North York, Ontario, Canada

Site Status

Pfizer Investigational Site

Oshawa, Ontario, Canada

Site Status

Pfizer Investigational Site

Oshawa, Ontario, Canada

Site Status

Pfizer Investigational Site

Ottawa, Ontario, Canada

Site Status

Pfizer Investigational Site

Saint Catherines, Ontario, Canada

Site Status

Pfizer Investigational Site

Saint Catherines, Ontario, Canada

Site Status

Pfizer Investigational Site

Sarnia, Ontario, Canada

Site Status

Pfizer Investigational Site

Thornhill, Ontario, Canada

Site Status

Pfizer Investigational Site

Thunder Bay, Ontario, Canada

Site Status

Pfizer Investigational Site

Thunder Bay, Ontario, Canada

Site Status

Pfizer Investigational Site

Toronto, Ontario, Canada

Site Status

Pfizer Investigational Site

Toronto, Ontario, Canada

Site Status

Pfizer Investigational Site

Toronto, Ontario, Canada

Site Status

Pfizer Investigational Site

Toronto, Ontario, Canada

Site Status

Pfizer Investigational Site

Windsor, Ontario, Canada

Site Status

Pfizer Investigational Site

Charlottetown, Prince Edward Island, Canada

Site Status

Pfizer Investigational Site

Montague, Prince Edward Island, Canada

Site Status

Pfizer Investigational Site

Amos, Quebec, Canada

Site Status

Pfizer Investigational Site

Chicoutimi, Quebec, Canada

Site Status

Pfizer Investigational Site

Cowansville, Quebec, Canada

Site Status

Pfizer Investigational Site

Greenfield Park, Quebec, Canada

Site Status

Pfizer Investigational Site

Greenfield Park, Quebec, Canada

Site Status

Pfizer Investigational Site

Greenfield Park, Quebec, Canada

Site Status

Pfizer Investigational Site

Laval, Quebec, Canada

Site Status

Pfizer Investigational Site

Laval, Quebec, Canada

Site Status

Pfizer Investigational Site

Laval, Quebec, Canada

Site Status

Pfizer Investigational Site

Le Gardeur, Quebec, Canada

Site Status

Pfizer Investigational Site

Montreal, Quebec, Canada

Site Status

Pfizer Investigational Site

Montreal, Quebec, Canada

Site Status

Pfizer Investigational Site

Montreal, Quebec, Canada

Site Status

Pfizer Investigational Site

Montreal, Quebec, Canada

Site Status

Pfizer Investigational Site

Plessisville, Quebec, Canada

Site Status

Pfizer Investigational Site

Québec, Quebec, Canada

Site Status

Pfizer Investigational Site

Saint-Eustache, Quebec, Canada

Site Status

Pfizer Investigational Site

Saint-Léonard, Quebec, Canada

Site Status

Pfizer Investigational Site

Salaberry Du Valleyfield, Quebec, Canada

Site Status

Pfizer Investigational Site

Sherbrooke, Quebec, Canada

Site Status

Pfizer Investigational Site

Ste. Foy, Quebec, Canada

Site Status

Pfizer Investigational Site

Vaudreuil, Quebec, Canada

Site Status

Pfizer Investigational Site

Regina, Saskatchewan, Canada

Site Status

Pfizer Investigational Site

Saskatoon, Saskatchewan, Canada

Site Status

Pfizer Investigational Site

Saskatoon, Saskatchewan, Canada

Site Status

Pfizer Investigational Site

Saskatoon, Saskatchewan, Canada

Site Status

Pfizer Investigational Site

Saskatoon, Saskatchewan, Canada

Site Status

Pfizer Investigational Site

Saskatoon, Saskatchewan, Canada

Site Status

Pfizer Investigational Site

St. John's, , Canada

Site Status

Pfizer Investigational Site

St. John's, , Canada

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Canada

References

Explore related publications, articles, or registry entries linked to this study.

Ur E, Langer A, Rabkin SW, Calciu CD, Leiter LA; CanACTFAST Study Investigators. Achieving cholesterol targets by individualizing starting doses of statin according to baseline low-density lipoprotein cholesterol and coronary artery disease risk category: the CANadians Achieve Cholesterol Targets Fast with Atorvastatin Stratified Titration (CanACTFAST) study. Can J Cardiol. 2010 Feb;26(2):80-6. doi: 10.1016/s0828-282x(10)70003-9.

Reference Type DERIVED
PMID: 20151053 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

A2581091

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Lipid-lowering Therapy Individualization
NCT03604471 COMPLETED PHASE4