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Protocol for CAMUS Delphi Study

Protocol for CAMUS Delphi Study: A Consensus on Reporting of Complications After Urological Surgeries

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04976946
Enrollment
750
Registered
2021-07-26
Start date
2021-08-12
Completion date
2023-12-31
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Complications; Urogenital, Postprocedural

Brief summary

Multi-staged, international Delphi study that aims to establish criteria for standardised complication reporting in Urology.

Detailed description

The CAMUS Delphi Study: A Consensus on Reporting of Complications After Urological Surgeries is a multi-staged, international Delphi study that aims to establish criteria for standardised complication reporting in Urology. The initial survey consists of a 12-part questionnaire that will aim to reach consensus on a wide range of contentious issues in Urological surgery using the frameworks of both the established Clavien-Dindo Classification (CDC) and the new CAMUS Classification. To ensure comprehensive and comparable complication reporting across centres worldwide, a conclusive uniform language for reporting complications must be created and subsequently integrated. Accurate reporting will allow for more precise allocation of resources, improve unit efficiency, and reduce healthcare burden, while providing clinicians with a better understanding of intra- and post-operative morbidity. If a comprehensive, homogenous reporting construct is integrated worldwide, the potential to build and develop a universal database with complications from all centres around the world will surely provide invaluable data to create new guidelines and recommendations, ultimately improving patient counselling and surgical quality of care.

Interventions

OTHERComprehensive questionnaire

Multi-staged, international Delphi study that aims to establish criteria for standardised complication reporting in Urology.

Sponsors

Melbourne Health
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

* Local and international consultant Urologists, accredited Urology trainees, consultant Anaesthetists and consultant ICU specialists will be invited to complete the survey. Critical care physicians who are primarily Urological anaesthetists or have experience in complication reporting will be targeted.

Exclusion criteria

* All other specialists that do not meet the inclusion criteria. * Under 18 years of age.

Design outcomes

Primary

MeasureTime frameDescription
Standardised complication reporting in Urology6 monthsEstablish criteria for standardised complication reporting in Urology

Countries

Australia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026