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. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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19 February 2015 |
Main ID: |
NCT00822419 |
Date of registration:
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13/01/2009 |
Prospective Registration:
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Yes |
Primary sponsor: |
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Public title:
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Percutaneous Ketamine Versus Lidocaine for Mid-Sternotomy
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Scientific title:
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Date of first enrolment:
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February 2009 |
Target sample size:
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75 |
Recruitment status: |
Not yet recruiting |
URL:
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http://clinicaltrials.gov/show/NCT00822419 |
Study type:
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Interventional |
Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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Phase:
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Phase 4
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Countries of recruitment
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Israel
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Contacts
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Name:
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Avi A Weinbroum, MD |
Address:
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Telephone:
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972-3-697-3237 |
Email:
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draviw@tasmc.health.gov.il |
Affiliation:
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Name:
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Avi A Weinbroum, MD |
Address:
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Telephone:
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972-3-697-3237 |
Email:
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draviw@tasmc.health.gov.il |
Affiliation:
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- all patients undergoing sternoromy for cardiac or chest sturgery
Exclusion Criteria:
- emergency surgery
Age minimum:
18 Years
Age maximum:
80 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Sternotomy
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Intervention(s)
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Drug: non-drug cream
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Drug: lidocaine
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Drug: ketamine
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Primary Outcome(s)
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Reduced postoperative pain
[Time Frame: 3 months]
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Secondary Outcome(s)
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Overall satisfaction
[Time Frame: 3 months]
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Secondary ID(s)
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0251-08-TLV
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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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