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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: |
NCT00512395 |
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Date of registration:
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06/08/2007 |
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Primary sponsor: |
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Public title:
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Influence of Epidural Analgesia in Elective Laparoscopic Colorectal Resections
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Scientific title:
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Influence of Epidural Analgesia in Elective Laparoscopic Colorectal Resections |
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Date of first enrolment:
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November 2004 |
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Target sample size:
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75 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT00512395 |
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Study type:
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Interventional |
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Study design:
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Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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Countries of recruitment
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Switzerland
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Contacts
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Name:
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Urs Zingg, 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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University Hospital, Basel, Switzerland |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- elective laparoscopic colorectal resection
Exclusion Criteria:
- emergency surgery
- preoperatively planned stoma formation
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Pain
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Intervention(s)
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Drug: epidural analgesia (Duracain/Fentanyl/Naropin)
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Drug: paracetamol, metmizole, morphine
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Primary Outcome(s)
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pain (VAS), cramps (VAS) and quantity of analgesics
[Time Frame: 8 days]
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Secondary Outcome(s)
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duration of postoperative ileus morbidity
[Time Frame: 6 months]
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Secondary ID(s)
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STZ 13/04
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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