Helsinki University Central Hospital
Helsinki, 00029, Finland
NCT Number: NCT02726932
The purpose of this study is to analyze the correlation between intra-abdominal view and patient recovery in secondary peritonitis, and to create a new classification based on these results. Additionally, a variety of inflammatory markers from blood samples will be collected in order to analyze their correlation with patient outcomes.
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Notify Me18 year and older
All sexes
Observational
Helsinki, 00029, Finland
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 90 days
Death within 90 days of primary operation for diffuse peritonitis
Time frame: 90 days
Intensive Care Unit admission and length of ICU treatment
Time frame: 90 days
Days in hospital postoperatively
Time frame: 90 days
Reoperations needed postoperatively
Time frame: 90 days
Postoperative complications according to Clavien-Dindo classification
Helsinki University Central Hospital
Other
Acronym: PERICLASS
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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