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Clinical Trials/NCT00677131
NCT00677131
Completed
N/A

Study of the Evaluation of Patient Education Efficacy: Reconstitution, Storage, and Administration of Oral Antibiotic Suspension From Powder Dosage Form at Pharmacy of National Taiwan University Hospital

National Taiwan University Hospital1 site in 1 country500 target enrollmentApril 2008
ConditionsInfection

Overview

Phase
N/A
Intervention
Not specified
Conditions
Infection
Sponsor
National Taiwan University Hospital
Enrollment
500
Locations
1
Primary Endpoint
Number of correct answer of questions that patient family make
Status
Completed
Last Updated
16 years ago

Overview

Brief Summary

The primary purpose of this study is to evaluate the patient education efficacy of the pharmacists in National Taiwan University Hospital. We randomize patient family into one of the following three groups:

  1. To read the package insert of the drug
  2. To read the education information provided by Pharmacy of NTUH
  3. Oral education provided by the pharmacist

Then we will evaluate the difference on patient knowledge of reconstitution, storage, and administration of oral antibiotic suspension from powder dosage form between these three groups.

Detailed Description

The primary purpose of this study is to evaluate the patient education efficacy of the pharmacists in National Taiwan University Hospital. We designed twelve questions about reconstitution, storage, and administration of oral antibiotic suspension from powder dosage form in a questionnaire. We will recruit pediatric patients who are prescribed one of the two oral antibiotics powder for suspension, Augmentin and Zithromax. We will randomize the family of these patients into one of the following three groups: 1. To read the package insert of the drug 2. To read the education information provided by Pharmacy of NTUH 3. Oral education provided by the pharmacist Then we will ask them the twelve questions in the questionnaire and record their answer. Eventually, we will be able to compare the number of the correct answer, and to evaluate the difference on patient knowledge of reconstitution, storage, and administration of oral antibiotic suspension from powder dosage form between these three groups.

Registry
clinicaltrials.gov
Start Date
April 2008
End Date
October 2009
Last Updated
16 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Family of pediatric patient who is prescribed one of the two oral antibiotics granule for suspension, Augmentin and Zithromax, in NTUH

Exclusion Criteria

  • Family of pediatric patient who can not read Chinese

Outcomes

Primary Outcomes

Number of correct answer of questions that patient family make

Time Frame: At the end of education

Secondary Outcomes

  • The type of the correct answer of question that patient family make(At the end of education)

Study Sites (1)

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