Day-case Endourology; Patient Experience

NCT06152679 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 15

Last updated 2023-12-01

No results posted yet for this study

Summary

A qualitative research study interviewing patients treated in hospitals across England. We will interview patients who have recently undergone one of the following operations as a day-case; transurethral bladder tumour resection (TURBT), transurethral resection of prostate (TURP) or transurethral enucleation of the prostate (TUEP). We are interested to find out about the experience for patients who go home on the day of surgery after they have had one of these operations. We hope that the findings will tell us about how to improve the experience for patients in future.

Patients undergoing day-case surgery at a range of different hospitals from across England with varying day-case rates will be interviewed. Hospitals in large city and more rural areas will be included. Interviews are anticipated to take place over a six month period. The study will end when "saturation" is achieved, whereby no new themes are identified through interviews. Saturation will be sought for each individual operation of interest.

Conditions

Interventions

OTHER

None - qualitative interviews

Qualitative interviews with patients asking about their experience of day-case endourology.

Sponsors & Collaborators

  • Royal Cornwall Hospitals Trust

    collaborator OTHER
  • North Bristol NHS Trust

    collaborator OTHER
  • Gloucestershire Hospitals NHS Foundation Trust

    collaborator OTHER
  • King's College Hospital NHS Trust

    collaborator OTHER
  • Portsmouth Hospitals NHS Trust

    collaborator OTHER_GOV
  • Royal Devon and Exeter NHS Foundation Trust

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-12-01
Primary Completion
2024-04-01
Completion
2024-10-01

Countries

  • United Kingdom

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06152679 on ClinicalTrials.gov