UCC-24HC014 UK PureWick™ At-Home Pilot Study

• Research type

  Research Study

• Full title

  An open-label pilot study conducted in the UK to evaluate the clinical benefits of the PureWick™ Female External Catheter System compared to indwelling urinary catheters in female patients receiving home-based care.

• IRAS ID

  363436

• Contact name

  Rebecca Willis

• Contact email

  rebecca.willis@nhft.nhs.uk

• Sponsor organisation

  BD

• Clinicaltrials.gov Identifier

  NCT07555548

• Duration of Study in the UK

  0 years, 9 months, days

• Research summary

  This is a pilot study for females who manage urinary incontinence with indwelling urinary catheters. The study aims to measure the clinical and quality of life benefits of the PureWick™ Female External Catheter System when compared to the current use of indwelling urinary catheters for urinary incontinence managed in the home setting.
  

• REC name

  South Central - Oxford C Research Ethics Committee

• REC reference

  26/SC/0021

• Date of REC Opinion

  8 Apr 2026

• REC opinion

  Further Information Favourable Opinion