Urinary Tract Infections Clinical Trial
— RxOUTMAPOfficial title:
Outcomes of Urinary Tract Infection Management by Pharmacists
NCT number | NCT03184818 |
Other study ID # | Pro00072493 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | June 16, 2017 |
Est. completion date | April 27, 2018 |
Verified date | May 2018 |
Source | University of Alberta |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
Pharmacists in some Canadian jurisdictions have recently been granted the ability to
prescribe for uncomplicated urinary tract infections (UTIs). Therefore, the purpose of this
study is to assess the impact that community pharmacists can have on the management of UTIs.
Pharmacists will identify potential study participants (patients) when they either present
with symptoms of a UTI (such as difficulty or painful urination, increased frequency or
urgency of urination) without a prescription for an antibiotic from another health care
provider, or when they present with a prescription for an antibiotic from another health care
provider to treat a UTI. For patients who consent to participate in the study, the pharmacist
will screen for eligibility and assess for appropriateness of treatment.
If the patient does not already have a prescription for an antibiotic from another health
care provider, the pharmacist will prescribe this for them if they meet certain criteria. If
they do already have a prescription from another health care provider, the pharmacist will
assess the appropriateness of the prescription and work with the patient to potentially
change it to make it more appropriate, if necessary. If the pharmacist identifies any
complicating factors that require a physician's assessment, the patient will be referred to
their physician. The enrolled patients will also have a 2-week follow-up to assess for
resolution of symptoms, unintended effects, and adherence to the treatment regimen. All data
will be collected in a web-based registry that will maintain the patient's confidentiality
outside of the pharmacy (i.e. patient initials, date of birth, and study identification (ID)
number will be the only patient identifiers collected by the researchers). A patient
satisfaction survey will also be administered via email.
Status | Completed |
Enrollment | 750 |
Est. completion date | April 27, 2018 |
Est. primary completion date | April 27, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 19 Years and older |
Eligibility |
Inclusion Criteria: - Patients presenting without a prescription for antibacterials from another health care practitioner with symptoms of urinary tract infection that is found to be uncomplicated. Or patients presenting with a prescription for an antibacterial from another health care practitioner that is found to either have uncomplicated urinary tract infection or asymptomatic bacteriuria. Exclusion Criteria: - Patients with complicated urinary tract infections or symptoms suggestive of pyelonephritis or systemic illness. |
Country | Name | City | State |
---|---|---|---|
Canada | EPICORE Centre, University of Alberta | Edmonton | Alberta |
Lead Sponsor | Collaborator |
---|---|
University of Alberta | Alberta Pharmacists Association, Horizon Health Network, Loblaw Companies Ltd., New Brunswick Pharmacists' Association, Pharmasave Drugs (Atlantic) Ltd., The Jean Coutu Group (PJC) Inc. |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of patients achieving clinical cure | Number of patients achieving sustained, full resolution of UTI symptoms, as described by the patient. This will be extracted from the registry database. | 2 weeks | |
Secondary | Antibacterials used | The name of antibacterials used to treat infection and the number of instances that each antibacterial was used. This will be extracted from the registry database. | 2 weeks | |
Secondary | Pharmacist interventions | Number of pharmacist interventions collectively and individually by the following types: antibacterial initiation, modification of antibacterial regimen, discontinuation of antibacterial regimen, and referral to physician. These will be extracted from the registry database. | 2 weeks | |
Secondary | Adherence | Patient adherence to initial recommendations and follow up. Pharmacists will ask and document if the patient took the antibacterial as prescribed, if they missed one or two doses, if they missed 50% or more doses, or if they didn't take at all. The number of patients reporting each of these will be extracted from the registry database. | 2 weeks | |
Secondary | Number of treatment failures | Number of patients experiencing either treatment failure or recurrence of symptoms | 2 weeks | |
Secondary | Reasons for treatment failures | The likely contributory factors of the patients experiencing treatment failures, such as less than ideal adherence, missed baseline complicating factor, resistant pathogen, complication (such as pyelonephritis), delay in accessing care, other, or no identifiable reason. The number of times that each of these were considered potentially contributory to treatment failure will be extracted from the registry database. | 2 weeks | |
Secondary | Patient satisfaction as determined by the modified consultation satisfaction questionnaire | Satisfaction of patients with the service provided by the pharmacists as determined by patients' responses to survey questions on a likert scale. | 2 weeks | |
Secondary | Access to care | Time to seen by a pharmacist (Arm 1) or physician (Arm 2) | 2 weeks | |
Secondary | Adverse events | Adverse events | 2 weeks |
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