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Abdominal Compartment Syndrome and Ruptured Aortic Aneurysm : Validation of a Predictive Test (SCA-AAR)

C

Centre Hospitalier Universitaire de Besancon

Status

Unknown

Conditions

Abdominal Compartment Syndrome

Treatments

Procedure: ruptured aortic aneurysm

Study type

Observational

Funder types

Other

Identifiers

NCT02859662
R/2015/49

Details and patient eligibility

About

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

Full 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.

Enrollment

165 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

10

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Central trial contact

Simon Rinckenbach, MD PhD

Data sourced from clinicaltrials.gov

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