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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: ClinicalTrials.gov
Last refreshed on: 12 December 2020
Main ID:  NCT03047057
Date of registration: 06/02/2017
Prospective Registration: Yes
Primary sponsor: Assiut University
Public title: Lidocaine Infusion in Radical Cystectomy
Scientific title: Effect of Lidocaine Infusion on Acute Rehabilitation After Radical Cystectomy
Date of first enrolment: March 3, 2017
Target sample size: 57
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT03047057
Study type:  Interventional
Study design:  Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Prevention. Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor).  
Phase:  Phase 2
Countries of recruitment
Egypt
Contacts
Key inclusion & exclusion criteria

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
Health Condition(s) or Problem(s) studied
Postoperative Ileus
Intervention(s)
Drug: IV normal saline
Drug: Lidocaine
Primary Outcome(s)
Postoperative return of gastrointestinal (GI) function [Time Frame: 15 day]
Secondary Outcome(s)
Postoperative Pain [Time Frame: 72 hours after surgery]
Secondary ID(s)
SM12017
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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