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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12 December 2020 |
Main ID: |
NCT03047057 |
Date of registration:
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06/02/2017 |
Prospective Registration:
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Yes |
Primary sponsor: |
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Public title:
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Lidocaine Infusion in Radical Cystectomy
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Scientific title:
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Effect of Lidocaine Infusion on Acute Rehabilitation After Radical Cystectomy |
Date of first enrolment:
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March 3, 2017 |
Target sample size:
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57 |
Recruitment status: |
Completed |
URL:
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https://clinicaltrials.gov/show/NCT03047057 |
Study type:
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Interventional |
Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Prevention. Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor).
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Phase:
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Phase 2
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Countries of recruitment
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Egypt
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- 45-75 yr ASA class I,II, and III Elective radical cystectomy
Exclusion Criteria:
- Allergy to the study medication, pre-existing chronic pain at any site requiring
treatment, Psychiatric disease, hepatic or renal impairment, seizure disorder
requiring medication within the previous 2 years
Age minimum:
45 Years
Age maximum:
65 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Postoperative Ileus
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Intervention(s)
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Drug: IV normal saline
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Drug: Lidocaine
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Primary Outcome(s)
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Postoperative return of gastrointestinal (GI) function
[Time Frame: 15 day]
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Secondary Outcome(s)
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Postoperative Pain
[Time Frame: 72 hours after surgery]
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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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