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Computer Tomography (CT) Trial of Acute Abdomen

Not Applicable
Completed
Conditions
Acute Abdomen
Registration Number
NCT00870766
Lead Sponsor
Kuopio University Hospital
Brief Summary

The purpose of this study is to determine the impact of routinely performed early CT scanning in terms of diagnostic accuracy, patient management and cost-effectiveness compared to current imaging practice in patients suffering from acute abdomen.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
250
Inclusion Criteria
  • age > 18
  • abdominal pain > 2h and < 7 days
Exclusion Criteria
  • pregnancy
  • acute abdominal trauma
  • allergy to iodinated contrast media
  • severe renal insufficiency
  • metformin medication combined with elevated plasma creatinin level
  • lack of cooperation (if informed consent is not possible)
  • abdominal pain combined with bleeding shock

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Diagnostic accuracyat discharge and/or 2-3 mo follow-up
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Kuopio University Hospital

🇫🇮

Kuopio, Finland

Kuopio University Hospital
🇫🇮Kuopio, Finland

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