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Validating the Novel Classification for the Assessment and Grading of Unexpected Events in Pediatric Surgery: The Clavien-Madadi Classification (ComPedS)

H

Hannover Medical School (MHH)

Status

Enrolling

Conditions

Complication of Surgical Procedure

Treatments

Other: Case Scenarios of complications to be ranked / classified according to classifications (for the severity grading of events)

Study type

Observational

Funder types

Other

Identifiers

NCT05778019
9557_BO_K_2021_2

Details and patient eligibility

About

Despite appraisal of the Clavien-Dindo classification in the pediatric surgical literature, some criticize the transfer of the grading systems for adults in a pediatric cohort without modifications. In a recent study it has been shown that few items of the classification do not offer additional information in pediatric cohorts and organizational and management errors have been integrated, not being part of the initial proposal by Dindo et al.

In a group of pediatric and general surgeons, methodologists and statisticians of the ERNICA network the Clavien-Dindo classification has been modified for the application in pediatric surgery. The aim is to test and validate the novel Clavien-Madadi classification in a pediatric surgical cohort.

Full description

Based on the protocol by Dindo et al. for the assessment of the international acceptability and reproducibility of the Clavien-Dindo classification, the aim is to circulate case scenarios (of complications/ unexpected events) within the ERNICA (European Reference Network for Rare Inherited Congenital Anomalies) network. Those case scenarios (15-20) should be graded by the respondents according to the Clavien-Dindo and Clavien-Madadi classification and preferences for future practice should be reported.

Milestones

  1. All members of the working group send the PI´s 1-2 case scenarios with unexpected events in the management and treatment of neonates (preferably congenital diseases) and children for each grade of the Clavien-Madadi classification
  2. All case scenarios will be circulated within the working group and will be ranked with a Likert scale (1 not accurate - 5 accurate) regarding the plausibility for an international survey
  3. A final proposal of 15-20 case scenarios will be circulated within the working group
  4. Circulating the case scenarios and the additional questionnaire via the ERNICA email distribution system and newsletter

Enrollment

20 estimated patients

Sex

All

Ages

1 day to 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Case scenarios of unexpected events
  • Case scenarios on neonatal surgery
  • Case scenarios on congenital malformations
  • Case scenarios with (re-)interventions
  • Case scenarios with organ impairment
  • Case scenarios with fatal result

Exclusion criteria

  • Complex constructed case scenarios
  • Case scenarios with adult patients
  • Case scenarios with multiple events

Trial design

20 participants in 1 patient group

Case Scenarios
Description:
No personal patient information is shared. The circulated case scenarios within the network will be constructed cases from the clinical practice, to serve representatively
Treatment:
Other: Case Scenarios of complications to be ranked / classified according to classifications (for the severity grading of events)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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