Observational Study On Compliance Of Statin Treatment Of Patients With High Blood Cholesterol Levels

NCT00673660

Last updated date
Study Location
Pfizer Investigational Site
Mecidiyekoy, Istanbul, 34394, Turkey
Contact
1-800-718-1021

FOR MORE INFORMATION

Contact a representative by phone, email, or visiting the study website. Please see the references below:

By phone

Pfizer Clinical Trials Contact Center

1-800-718-1021

By email

Contact

[email protected]

Call Now

Eligibility Criteria
condition
The disease, disorder, syndrome, illness, or injury that is being studied.
Dyslipidemia
Sex
Females and Males
Age
Pediatric Trials: 0-17 Years
Adult Trials: 18+ Years
18 + years
Inclusion Criteria
The factors, or reasons, that allow a person to participate in a clinical study.
Show details

- Patients diagnosed with dyslipidemia and taking or planning to take statin treatment.

- Patients living in the same city of the study center. o Patients aged 18 years and over.

Exclusion Criteria
The factors, or reasons, that prevent a person from participating in a clinical study.
Show details


- Patients with severe systemic disease


- Patients with alcohol and drug addiction and/or mental disease


- Patients nursing or pregnant, or planning to get pregnant during the study

NEED INFO?

Questions about a trial? Call or email to reach a Pfizer Clinical Trial Contact Center Representative

Pfizer Clinical Trials Contact Center

1-800-718-1021

[email protected]

TRY A NEW SEARCH

Search for Clinical Trials by condition, keyword or trial number. Share your location or enter your city or zip code to find studies near you.

Based on your search, you may also be interested in

DyslipidemiaEffect of CP-778,875 on HDL-C in Subjects With Abnormal Lipid Levels and Type 2 Diabetes. NCT00326326
  1. Anniston, Alabama
  2. Huntsville, Alabama
  3. Greenbrae, California
  4. Los Angeles, California
  5. Walnut Creek, California
  6. DeFuniak Springs, Florida
  7. Destin, Florida
  8. Jupiter, Florida
  9. Melbourne, Florida
  10. Atlanta, Georgia
  11. Conyers, Georgia
  12. Chicago, Illinois
  13. Iowa City, Iowa
  14. Lexington, Kentucky
  15. Baltimore, Maryland
  16. Springfield, Missouri
  17. Omaha, Nebraska
  18. Las Vegas, Nevada
  19. Mount Vernon, New York
  20. Oklahoma City, Oklahoma
  21. Tulsa, Oklahoma
  22. Kingsport, Tennessee
  23. Bryan, Texas
  24. Houston, Texas
  25. San Antonio, Texas
  26. Newport News, Virginia
  27. Richmond, Virginia
  28. Richmond, Virginia
  29. Richmond, Virginia
  30. Yakima, Washington
  31. Milwaukee, Wisconsin
ALL GENDERS
30 Years+
years
MULTIPLE SITES
DyslipidemiaA Study to Evaluate the Efficacy of a Counselling and Advisory Care for Health (COACH) Program in Dyslipidemic Patients. NCT00708370
  1. Jitra, Kubang Pasu, Kedah
  2. Kulim, Kedah
  3. Sik, Kedah
  4. Kubang Kerian, Kelantan
  5. Cheras, Kuala Lumpur
  6. Cheras, Kuala Lumpur
  7. Nilai, Negeri Sembilan
  8. Tampin, Negeri Sembilan
  9. Bagan Serai, Perak
  10. Lenggong, Perak
  11. Slim River, Perak
  12. Kapar, Selangor
  13. Petaling Jaya, Selangor
  14. Puchong, Selangor
  15. Sungai Buloh, Selangor
  16. Kemaman, Terengganu
  17. Kerteh, Kemaman, Terengganu
  18. Kuala Lumpur, Wilayah Persekutuan
  19. Kuala Lumpur,
  20. Kuala Lumpur,
  21. Melaka,
  22. Shah Alam,
ALL GENDERS
18 Years+
years
MULTIPLE SITES
DyslipidemiaObservational Study On Compliance Of Statin Treatment Of Patients With High Blood Cholesterol Levels NCT00673660
  1. Mecidiyekoy, Istanbul
  2. Bolu,
  3. Haseki/Istanbul,
  4. Istanbul,
  5. Istanbul,
ALL GENDERS
18 Years+
years
MULTIPLE SITES
Advanced Information
Descriptive Information
Brief Title Observational Study On Compliance Of Statin Treatment Of Patients With High Blood Cholesterol Levels
Official Title Assessment Of Statin Treatment Compliance In Dyslipidemia Patients: An Observational Study
Brief Summary The purpose of the study is to show the compliance rates of the patients to statin treatment and the reasons of non-compliance.
Detailed Description Not Provided
Study Type Observational
Study Design Observational Model: Cohort
Time Perspective: Prospective
Target Follow-Up Duration Not Provided
Biospecimen Retention:   None Retained
Description:
No biospecimen is retained
Sampling Method Non-Probability Sample
Study Population Patients diagnosed with dyslipidemia and taking or planning to take statin treatment. Patients living in the same city of the study center. Patients aged 18 years old and over.
Condition Dyslipidemia
Intervention Behavioral: Patient Compliance
Compliance of patients to statin treatment and reasons of compliance or non compliance will be obtained by Patient Reported Outcomes (PROs) every 3 months.
Study Groups/Cohorts Statins
Patients with dyslipidemia who are taking or planning to take a statin treatment (Atorvastatin, Fluvastatin, Prevastatin, Rosuvastatin, Simvastatin or generics).
Intervention: Behavioral: Patient Compliance
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Completed
Actual Enrollment
 (submitted: December 11, 2009)
375
Original Estimated Enrollment
 (submitted: May 1, 2008)
670
Actual Study Completion Date October 2009
Actual Primary Completion Date October 2009   (Final data collection date for primary outcome measure)
Eligibility Criteria

Inclusion Criteria:

  • Patients diagnosed with dyslipidemia and taking or planning to take statin treatment.
  • Patients living in the same city of the study center. o Patients aged 18 years and over.

Exclusion Criteria:

  • Patients with severe systemic disease
  • Patients with alcohol and drug addiction and/or mental disease
  • Patients nursing or pregnant, or planning to get pregnant during the study
Sex/Gender
Sexes Eligible for Study:All
Ages 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers No
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries Turkey
Removed Location Countries  
 
Administrative Information
NCT Number NCT00673660
Other Study ID Numbers A2581156
Has Data Monitoring Committee No
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement Not Provided
Responsible Party Director, Clinical Trial Disclosure Group, Pfizer, Inc.
Study Sponsor Pfizer
Collaborators Not Provided
Investigators
Study Director:Pfizer CT.gov Call CenterPfizer
PRS Account Pfizer
Verification Date December 2009