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Main
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Note: This record shows only the 20 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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17 October 2012 |
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Main ID: |
NCT00910052 |
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Date of registration:
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28/05/2009 |
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Primary sponsor: |
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Public title:
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Fibrin Sealant in Renal Transplantation
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Scientific title:
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Routine Use of Fibrin Sealant Does Not Reduce Postoperative Wound Complications in Patients Undergoing Renal Transplantation: A Randomized Controlled Trial |
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Date of first enrolment:
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May 2003 |
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Target sample size:
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141 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT00910052 |
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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: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Prevention
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Countries of recruitment
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United States
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- All renal transplant recipients
Exclusion Criteria:
- Patients declining study
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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Renal Transplantation
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Intervention(s)
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Device: Tisseelä fibrin sealant
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Primary Outcome(s)
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presence of postoperative fluid collection
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Secondary Outcome(s)
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wound dehiscence
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wound infection
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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