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Abdominal Compartment Syndrome and Ruptured Aortic Aneurysm : Validation of a Predictive Test

Abdominal Compartment Syndrome and Ruptured Aortic Aneurysm : Validation of a Predictive Test

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02859662
Acronym
SCA-AAR
Enrollment
165
Registered
2016-08-09
Start date
2016-09-30
Completion date
2019-03-31
Last updated
2017-11-07

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

Conditions

Abdominal Compartment Syndrome

Keywords

abdominal compartment syndrome, abdominal aortic aneurysm, ruptured aneurysm

Brief summary

It is an observational study on ruptured abdominal aortic aneurysm and abdominal compartment syndrome. the aim of this study is to assess the qualities of a predictive score on the occurence of this syndrome after surgery of ruptured aortic aneurysm

Detailed description

Despite improved management techniques of ruptured abdominal aortic aneurysm, especially in vascular surgery, the mortality rate has not decreased these last years. The abdominal compartment syndrome (ACS) has been clearly identified as one of the main etiologies of mortality after ruptured aortic aneurysm. The mortality grow up with ACS in this population. So, the investigators want to screen abdominal compartment syndrome in the operative room. It is an observational study on ruptured abdominal aortic aneurysm and abdominal compartment syndrome. the aim of this study is to assess the qualities of a predictive score on the occurence of this syndrome after surgery of ruptured aortic aneurysm Later the aim of a future study will be to screen ACS and manage patient as soon as possible to avoid it.

Interventions

PROCEDUREruptured aortic aneurysm

All patients with ruptured abdominal aortic aneurysm may be included in this study, whatever the surgical treatment.

Sponsors

Centre Hospitalier Universitaire de Besancon
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

* over 18 * to be hospitalized in participating hospitals * ruptured aneurysm confirmed and operated

Exclusion criteria

* pregnancy * patients with bladder tumor or bladder surgery or trauma bladder can distort bladder pressure measurement * cystectomy * patients died before arrival in the operating room * patients died during surgery or within one hour of the initial surgical procedure * patient whose abdominal closure at the end of the procedure is impossible

Design outcomes

Primary

MeasureTime frameDescription
a predictive score on the appearance of an abdominal compartment syndrome after a surgical treatment of a ruptured abdominal aortic aneurysm30 daysscore with criteria

Secondary

MeasureTime frameDescription
30 days mortality rate30 daysMortality
the duration of hospitalisation (intensive care unit stay and total hospital stay)30 daysDuration in day of hospitalisation

Countries

France

Contacts

Primary ContactSimon Rinckenbach, MD PhD
srinckenbach@chu-besancon.fr

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026