Comprehensive Complication Index in the Classification of Complications of Percutaneous Nephrolithotomy

NCT05351632 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 644

Last updated 2022-04-28

No results posted yet for this study

Summary

Postoperative complications should be reported systematically, objectively and reproducibly. The Clavien-Dindo Classification (CDC), first described in 2004, is the most popular classification system still in use today for assessing perioperative morbidity and mortality. In 2018, the European Association of Urology (EAU) validated this classification, which was originally defined for general surgery operations, for urological operations as well. There are aspects of the CDC that can be critical and weak. The CDC's main weakness is that in the vast majority of studies it only considers the most serious complications. Minor complications are often overlooked and the overall complication burden is therefore underestimated. Because of this vulnerability, it is difficult to compare complications from different patients. For example, it cannot be determined whether a patient with two Grade I complications has higher postoperative morbidity than a patient with one Grade II complication. To address these limitations, the Comprehensive Complications Index (CCI) was defined in 2013 as a new and more comprehensive scoring system for surgical complications.

The CCI is essentially an index based on the CDC, but sums all postoperative complications by severity and scores them on an interval scale. It is scored from 0 (no complications) to 100 (patient's death) for each patient.

CCI in Urology Practice; Validated for Radical Cystectomy, Radical Prostatectomy, Radical Nephroureterectomy, Partial Nephrectomy.

In recent years, validation studies of this index have been carried out in endourological surgeries.

Conditions

  • Complications, Postoperative

Sponsors & Collaborators

  • Zonguldak Bulent Ecevit University

    collaborator OTHER
  • Ankara University

    collaborator OTHER
  • Inonu University

    collaborator OTHER
  • Istanbul University

    collaborator OTHER
  • Acibadem University

    collaborator OTHER
  • Eskisehir Osmangazi University

    collaborator OTHER
  • Başakşehir Çam & Sakura City Hospital

    collaborator OTHER_GOV
  • Koç University

    collaborator OTHER
  • Izmir Metropolitan Municipality Esrefpasa Hospital

    collaborator UNKNOWN
  • Alanya Alaaddin Keykubat University

    collaborator OTHER
  • Cukurova University

    collaborator OTHER
  • Ondokuz Mayıs University

    collaborator OTHER
  • Dokuz Eylul University

    collaborator OTHER
  • Samsun Education and Research Hospital

    collaborator OTHER
  • Gazi University

    collaborator OTHER
  • Hacettepe University

    collaborator OTHER
  • Abant Izzet Baysal University

    collaborator OTHER
  • Ankara Training and Research Hospital

    collaborator OTHER
  • Hitit University

    collaborator OTHER
  • Baskent University

    collaborator OTHER
  • Marmara University

    lead OTHER

Principal Investigators

  • Reha GİRGİN, Assist.Prof. · Zonguldak Bulent Ecevit University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-05-01
Primary Completion
2023-04-30
Completion
2023-04-30

Countries

  • Turkey (Türkiye)

Study Locations

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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 NCT05351632 on ClinicalTrials.gov