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NCT01876667 · ClinicalTrials.gov registry record · NA

An Evaluation of Clinical Pharmacist-led Intervention on Clinical Outcomes in Patients With Ischemic Stroke

A NA study, sponsored by Kaiser Permanente.

Completed
Registry status
NA
Development phase
141
Enrollment target

NCT01876667: Completed NA study, sponsored by Kaiser Permanente.

NCT01876667 is a NA study that has completed, run by Kaiser Permanente. The registered enrollment target is 141 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01876667, a NA study, has completed, sponsored by Kaiser Permanente.

COMPLETED
Registry status
NA
Development phase
141 participants
Enrollment target

Study Summary

Clinical pharmacy specialists are in an ideal position to assist medical teams in the management of patients with ischemic stroke. Given their extensive and specialized knowledge regarding medication efficacy, safety, and cost-effective use as well as their ability to critically review, interpret and apply the results from clinical studies to patient care, clinical pharmacy specialists have the potential to have a significant impact on stroke care delivery. There are numerous opportunities for clinical pharmacy specialists to become more extensively involved in the delivery of care to these high-risk patients. However, to-date there are few studies demonstrating the impact of clinical pharmacy specialists on outcomes of patients with stroke Stroke is the third leading cause of death in the United States (U.S.) and the most common life-threatening neurologic disorder.1 Stroke is a leading cause of long-term disability and results in significant individual and societal financial burdens. In 2006, stroke accounted for 1 of every 18 deaths and ischemic stroke accounted for 87% of all strokes.1 In the U.S., out of the approximately 795,000 people who develop a stroke each year, approximately 185,000 (23%) are recurrent events.1 After the first year, the average annual risk for recurrent stroke is 4%.2 Patients who survive at least 30 days after a first-ever stroke, have an average annual risk of death of 9.1%, much of the risk due to nonstroke cardiovascular disease. Despite the evidence supporting the use of various therapeutic interventions within the ischemic stroke population, a significant proportion of patients continue to have uncontrolled risk factors and remain undertreated.26-30 A recent prospective study of more than 4933 high-risk patients reported that, as compared to patients with coronary artery disease, patients with cerebrovascular disease are undertreated and thus less likely to achieve blood pressure (45.3% vs. 57.3%; p\<0.001) and lipid (19.4% vs. 30

Primary Outcome

The outcome measures selected for the study are based on AHA/ASA guidelines for prevention of stroke in patients with ischemic stroke or transient ischemic attack.19,20 The surrogate measures to be evaluated are the "ABCs" which include Antiplatelet/antithrombotic therapy, Blood pressure control, Cholesterol control, and Smoking cessation. These variables will be evaluated at various time points during the study in part to evaluate the CPCRS processes of care for attaining surrogate measures in

Interventions

  • OTHER Placebo
  • OTHER Intervention (CPCRS) Group

Trial Details

FieldValue
Enrollment Target 141 participants
Start Date 2010-07
Est. Completion 2018-11-14
Phase NA
Kaiser Permanente

294 total trials

What the finished NCT01876667 record still lists

NCT01876667 is an interventional study that assigns participants to a tested intervention. The registered 141 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT01876667 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01876667 about?

NCT01876667 is a clinical study titled "An Evaluation of Clinical Pharmacist-led Intervention on Clinical Outcomes in Patients With Ischemic Stroke". Clinical pharmacy specialists are in an ideal position to assist medical teams in the management of patients with ischemic stroke. Given their extensive and specialized knowledge regarding medication efficacy, safety, and cost-effective use as well as their ability to critically review, interpret an...

What is the current status of trial NCT01876667?

This trial is currently completed. It is a NA study. The enrollment target is 141 participants. The study started on 2010-07. Estimated completion is 2018-11-14.

What interventions are being tested in trial NCT01876667?

The interventions under investigation include: Placebo (OTHER), Intervention (CPCRS) Group (OTHER).

Who is sponsoring clinical trial NCT01876667?

This trial is sponsored by Kaiser Permanente, which has 294 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01876667's enrollment target sits among peer trials

141 712th of 2000 higher than 1,288 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01876667, the US trial registry maintained by the National Library of Medicine. NCT01876667 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.