Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00870766
Other study ID # KUH5200617
Secondary ID
Status Completed
Phase N/A
First received March 26, 2009
Last updated September 13, 2010
Start date January 2009
Est. completion date June 2010

Study information

Verified date September 2010
Source Kuopio University Hospital
Contact n/a
Is FDA regulated No
Health authority Finland: Ethics Committee
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 250
Est. completion date June 2010
Est. primary completion date January 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Procedure:
Abdominal contrast-enhanced CT scanning
Contrast-enhanced (iohexol 350 mgI/ml, 100 ml IV) CT scanning

Locations

Country Name City State
Finland Kuopio University Hospital Kuopio

Sponsors (1)

Lead Sponsor Collaborator
Kuopio University Hospital

Country where clinical trial is conducted

Finland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Diagnostic accuracy at discharge and/or 2-3 mo follow-up No
See also
  Status Clinical Trial Phase
Recruiting NCT04196244 - Intravenous Contrast Computed Tomography Versus Native Computed Tomography in Patients With Acute Abdomen and Impaired Renal Function Phase 4
Withdrawn NCT01044173 - Plain Magnetic Resonance (MR) in the Assessment of Patients With Acute Abdomen N/A
Active, not recruiting NCT06154603 - Upper Gastrointestinal Perforations: a Nationwide Registry-based Study
Recruiting NCT06182488 - Enhanced Recovery After Surgery (ERAS) in Patients Undergoing Emergency Laparotomy N/A
Completed NCT05295251 - The Commonest Medical, Surgical, and Oncological Causes of Acute Abdomen in Adults With COVID-19. A Prospective Observational Study.
Not yet recruiting NCT05407922 - Laparoscopic Value in the Management of Acute Abdomen During Pregnancy
Recruiting NCT02467959 - Diagnostic Accuracy of Emergency Physician Performed Bedside Ultrasound in Suspected Acute Appendicitis N/A
Completed NCT01911702 - Different Fluidic Strategy in Patients With Acute Abdomen : The Sure Volume Phase 2
Completed NCT05419440 - Laparoscopic Drainage Versus Interventional Radiology In Management Of Appendicular Abscess : N/A
Completed NCT05004532 - Transversus Abdominis Plane Block in Acute Appendicitis Pain Managment
Completed NCT05591495 - The Role of Laparoscopy in Upper Abdominal Surgical Emergencies in Adults: A Retrospective Observational Study.
Completed NCT03262025 - Primary Cecal Pathologies Presenting as Acute Abdomen N/A
Active, not recruiting NCT03549624 - Standardized Perioperative Management of Patients Operated With Acute Abdominal Surgery in a High-risk Emergency Setting
Recruiting NCT06320886 - Role of Ultrasonography in Acute Abdomen in Adults in Correlation to Computed Tomography Scan
Completed NCT01982708 - A Prospective Study of a Haptic Device Evaluation of the Acute Abdomen N/A
Not yet recruiting NCT04577339 - The Best Care for Abdominal Emergencies Study
Completed NCT04662242 - The Prognostic Impact of Selenium On Critical Surgical Patients Phase 4
Completed NCT04966780 - Refeeding Like Syndrome in Acute Disease
Enrolling by invitation NCT03096665 - Effectiveness of Point of Care Blood Analysis Obtained From Skin Puncture Blood N/A