Skip to main content
OpenTrials
Completed

NCT Number: NCT01222182

Statin Interchange by Pharmacist Collaborative Practice Agreement (CPA)

A group of ~ 225 patients were switched from atorvastatin to an equivalent statin either by their physicians usual management or by an collaborative pharmacist coordinated process. We will compare the results of pharmacist process to the standard medical practice to find potentially which process is more effective, safer and efficient. We are surveying a total of 35 physicians, 12 using the pharmacist coordinated process and 23 not, comparing their satisfaction of the 2 processes.

Completed

Looking for future studies?

Notify Me

Key information

Age range

25 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Mayo Clinic in Rochester

Rochester, Minnesota, 55905, United States

About this study

This study is a retrospective analysis of patients converted from atorvastatin to another equivalent statin. It is observational because the patients were all on atorvastatin, had been informed by their prescription drug plan that it would not be covered, and that if agreed they would be changed to an equivalent that is covered by their plan. The patients were either converted with the help of pharmacist by collaborative practice agreement (CPA)or upon contacting their physician requesting a different medication. We are comparing the percentage first converted to the equivalent dose in each group and whether patients continued to be at hyperlipidemia treatment goal after the interchange.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

225 insured eligible subjects, 35 PCIM physicians

Treatment and study plan

atorvastatin

Drug

All patients desired to change atorvastatin 10, 20mg to an equivalent that is covered by their prescription plan. This is accomplished by either pharmacists by MD/Pharmacist practice agreement or physicians in usual practice

Other names: atorvastatin, (Lipitor®),, interchanged to simvastatin, pravastatin

Primary outcomes

  1. Determine if a process of pharmacist practice agreement is effective in changing from atorvastatin 10, 20mg to a therapeutic equivalent dose.

    Time frame: 3 to 9 months after conversion from atorvastatin

    We compared doses selected for therapeutic equivalency for the new statin Did the process result in selecting a safe and effective statin alternative?

Secondary outcomes

  1. Was the process regarded as efficient and satisfying to physician compared to usual practice.

    Time frame: 5 months post conversion

    A satisfaction survey of physicians who utilized the pharmacist collaborative practice agreement(CPA) will be compared to satisfaction of phycians who were not able to use the CPA. Was the process regarded as efficient and satisfying to physician compared to usual practice.

  2. Did the patients' low density lipoprotein(LDL) cholesterol require further statin dose intervention?

    Time frame: 6-12 months

    Of patients who had a follow up LDL cholesterol, how many required another intervention after failing to stay within treatment goal. Physicians usually measure each of these patients within 3 months of a change of treatment and annually thereafter. We will look at follow up LDL cholesterol and liver function test (LFT) as recommended.

Sponsors and collaborators

Lead sponsor

Mayo Clinic

Other

Registry information

Official study title

Statin Therapeutic Interchange by Pharmacist Collaborative Practice Process

Important dates

Study start
2009
Primary completion
2011
Study completion
2011
First posted
Oct 18, 2010
Registry last updated
May 28, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.