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Immediate management of patients with ruptured aneurysm: open versus endovascular repair

Completed
Conditions
Abdominal aortic aneurysm
Circulatory System
Aortic aneurysm and dissection
Registration Number
ISRCTN48334791
Lead Sponsor
Imperial College London (UK)
Brief Summary

2009 protocol in: http://www.ncbi.nlm.nih.gov/pubmed/19464199 2009 protocol in: http://www.ncbi.nlm.nih.gov/pubmed/20184048 2014 results in: http://www.ncbi.nlm.nih.gov/pubmed/24418950 2014 results in: http://www.ncbi.nlm.nih.gov/pubmed/24469620 2014 results in: http://www.ncbi.nlm.nih.gov/pubmed/24485843 2015 results in: http://www.ncbi.nlm.nih.gov/pubmed/25627357 2015 results in: http://www.ncbi.nlm.nih.gov/pubmed/25855369 2015 results in: http://www.ncbi.nlm.nih.gov/pubmed/26104471 2015 results in: http://www.ncbi.nlm.nih.gov/pubmed/25981698 2017 results in: http://www.ncbi.nlm.nih.gov/pubmed/29138135 2018 results in: http://www.ncbi.nlm.nih.gov/pubmed/29503083 2018 results in: http://www.ncbi.nlm.nih.gov/pubmed/29860967

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
600
Inclusion Criteria

1. Both males and females, over the age of 50 years
2. Clinical suspicion of ruptured abdominal aortic aneurysm after review in Accident and Emergency (or other hospital unit)

Exclusion Criteria

1. Patients with known connective tissue disorders (e.g., Marfan syndrome) where endovascular repair may not be beneficial
2. Patients with known previous repair of an abdominal aortic aneurysm, because procedures either open or endovascular are likely to be very complex and there are no guidelines for anatomical restriction to repair
3. Deeply unconscious and moribund patients since the chances of recovery are minimal

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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