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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.

Contact Information:

Dr Gail Hayward
+44 (0)1865 289357
gail.hayward@phc.ox.ac.uk


Study Location:

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Be Part of Research - Trial Details - CONDUCT - Collection devices to reduce urine contamination

CONDUCT - Collection devices to reduce urine contamination

Not Recruiting

Open to: Female

Age: Adult

Medical Conditions

Urinary tract infections


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


Urinary tract infections (UTIs) are common infections that can affect the bladder, kidneys and the tubes that connect the bladder and kidneys together (the urinary tract). Symptoms include needing to urinate more than usual, pain while urinating, a sudden urge to urinate, feeling that the bladder is never fully empty, abdominal pain, cloudy urine and generally not feeling very well. Anyone can get a UTI but they are more common in women than men. 1 in 10 women see their GP each year because they have a UTI. When someone goes to see their GP with UTI symptoms they may be asked to provide a urine sample which can be sent to the laboratory for urine culture, in order to find out if there are any bacteria present. However, up to 30% of urine samples are contaminated by bacteria which normally live on the body. A contaminated sample cannot rule out infection or prove there is an infection. Another sample will need to be sent, and the delay may increase the length of time a patient experiences symptoms and mean they take extra courses of antibiotics; this could result in infections resistant to antibiotics in the future. If every contaminated urine culture was repeated this would cost over ÂŁ14 million annually in England and Wales. This study will test whether using urine collection devices to produce urine samples can reduce the chances of contamination. There are two urine collection devices available on the NHS; the Whizaway Midstream and the Peezy. Both claim that they reduce contamination, but this has not been properly tested. The devices are funnel shaped containers which use two different methods to collect the urine sample.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

01 Oct 2016 20 Aug 2018

Publications

2022 Results article in https://pubmed.ncbi.nlm.nih.gov/34990390/ (added 09/06/2023)

Participants are randomly allocated to one of three groups Those in group 1 are given standard
Instructions and asked to pass urine into a standard 30ml sterile universal container. Participants in group 2 are given the Peezy Urine collection device to collect their urine sample. Participants in group 3 are asked to provide their urine sample using the Whizaway midstream Urine collection device. All samples collected from each participant is checked for contamination in a laboratory.
Participants are also asked to complete a questionnaire 14 days after they begin the study and will be contacted by telephone 14-21 days and asked for their views.


Women (aged over 18) and presenting to their doctor with symptoms that suggest they have a UTI.

You can take part if:



You may not be able to take part if:


The participant may not enter the study if ANY of the following apply:1. Patients who are currently taking antibiotics or have taken antibiotics in the last 7 days2. Patients with indwelling catheters or using intermittent self-catheterisation3. Patients unable to give informed consent 4. Previously recruited to the trial


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

This study does not pose significant risks or benefits to participants associated with taking part.


The study is sponsored by University of Oxford and funded by National Institute for Health Research.




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Read full details for Trial ID: ISRCTN68511881
Last updated 09 June 2023

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