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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT00597363 |
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Date of registration:
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09/01/2008 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Neptune Pad ® Compared to Conventional Manual Compression
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Scientific title:
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Neptune Pad ® Compared to Conventional Manual Compression for Access Site Management After Peripheral Percutaneous Transluminal Procedures |
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Date of first enrolment:
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January 2006 |
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Target sample size:
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201 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT00597363 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
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Phase:
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N/A
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Countries of recruitment
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Austria
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Contacts
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Name:
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Martin Schillinger, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Professor |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- All inguinal punctures (common femoral, superficial femoral and deep femoral artery,
antegrade and retrograde access) were included.
- No specific limitations of anti-platelet or anti-coagulant medication were specified.
Exclusion Criteria:
- Patients with extreme obesity (BMI above 35 kg/m2) were not included according to the
manufactures' recommendations.
- Furthermore, patients with known hypersensitivity to components of the device were
not eligible
Age minimum:
N/A
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Postoperative Hemorrhage
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Intervention(s)
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Other: conventional manual compression
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Device: Neptune P.A.D. (R)
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Secondary ID(s)
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EK 433/2004
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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