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Intra-abdominal View and Inflammatory Markers in Secondary Peritonitis - Correlation to Recovery

Intra-abdominal View and Inflammatory Markers in Secondary Peritonitis - Correlation to Recovery

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02726932
Acronym
PERICLASS
Enrollment
283
Registered
2016-04-04
Start date
2016-03-30
Completion date
2018-03-30
Last updated
2019-01-16

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

Conditions

Peritonitis

Keywords

Peritonitis, Inflammatory Markers, Patient Outcome Assessment, Classification, Multiple Organ Failure, Intraabdominal Infections

Brief summary

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.

Interventions

OTHERNo intervention, merely observational

Sponsors

Helsinki University Central Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* adult patients \> 18 years old * operated for complicated intra-abdominal infection

Exclusion criteria

* another diagnosis requiring ICU level care at the same time * acute pancreatitis * acute mesenteric ischaemia due to occlusion in superior mesenteric artery or vein * peritonitis due to timely diagnosed trauma * missing informed consent or inability to understand it

Design outcomes

Primary

MeasureTime frameDescription
Mortality90 daysDeath within 90 days of primary operation for diffuse peritonitis
ICU admission90 daysIntensive Care Unit admission and length of ICU treatment
Length of hospitalization90 daysDays in hospital postoperatively
Reoperations90 daysReoperations needed postoperatively
Complications90 daysPostoperative complications according to Clavien-Dindo classification

Countries

Finland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026