Skip to main content
Clinical Trials/ISRCTN65200697
ISRCTN65200697
Completed
未知

Point of care testing for urinary tract infection in primary care: Stages 3 & 4 - a randomised controlled trial

Cardiff University (UK)0 sites614 target enrollmentSeptember 10, 2013

Overview

Phase
未知
Intervention
Not specified
Conditions
Topic: Primary Care Research Network for England
Sponsor
Cardiff University (UK)
Enrollment
614
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

  1. 2014 protocol in: http://www.ncbi.nlm.nih.gov/pubmed/25425162 2. 2018 results in https://www.ncbi.nlm.nih.gov/pubmed/29483078 (added 24/01/2019) 3. 2019 results in https://pubmed.ncbi.nlm.nih.gov/31873085/ (added 11/11/2020)
Registry
who.int
Start Date
September 10, 2013
End Date
November 1, 2015
Last Updated
5 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Cardiff University (UK)

Eligibility Criteria

Inclusion Criteria

  • 1\. Women aged 18 years and above presenting with suspected uncomplicated urinary tract infection.
  • 2\. Presenting with at least one of three key urinary tract symptoms (dysuria, urgency including nocturia, and frequency)
  • 3\. Able to provide informed consent and willing to complete a patient diary.

Exclusion Criteria

  • Added 12/12/2016:
  • 1\. Terminally ill
  • 2\. Currently receiving treatment for life\-threatening cancer (basal cell carcinoma, for example, excluded)
  • 3\. Other severe systemic symptoms, such as high fever, renal angle pain, rigors
  • 4\. On long\-term antibiotic treatment or have received antibiotics for urinary tract infection within the past four weeks
  • 5\. Has had bladder surgery (including cystoscopy) within the past four weeks
  • 6\. Known or likely to have significant immune compromise (i.e. known immunodeficiency state, on long\-term corticosteroid or chemotherapy treatment, insulin dependent diabetes)
  • 7\. Known functional or anatomical abnormalities of the genitourinary tract
  • 8\. History of pyelonephritis
  • 9\. Known pregnancy

Outcomes

Primary Outcomes

Not specified

Similar Trials