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Day-case Endourology; Enablers, Barriers, Unexpected Outcomes

NCT06152666 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 15

Last updated 2023-12-01

No results posted yet for this study

Summary

A qualitative research study conducted in hospitals across England, in which staff members will be interviewed. We will interview staff who are directly or indirectly involved in delivering care for patients undergoing the operations of interest; namely bladder tumour resection, prostate resection or enucleation, and ureteroscopy for upper urinary tract stones. We hope to find out the reasons why some hospitals can perform day-case surgery with very high rates, and why others do not. We also hope to find out about any unexpected outcomes observed when performing day-case surgery for the operations of interest.

Staff working in 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 assessed. 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

These are qualitative interviews and involve no intervention

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

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

Diseases

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 NCT06152666 on ClinicalTrials.gov