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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. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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24 January 2022 |
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Main ID: |
NCT02984800 |
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Date of registration:
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03/12/2016 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Effectiveness of Single Paravertebral Blockade Injection for Herniorrhaphy in Children
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Scientific title:
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The Anesthetic and Analgesic Effectiveness of Single Paravertebral Blockade Injection for Herniorrhaphy in Children |
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Date of first enrolment:
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December 2016 |
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Target sample size:
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100 |
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Recruitment status: |
Recruiting |
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URL:
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https://clinicaltrials.gov/show/NCT02984800 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Other. Masking: Triple (Participant, Care Provider, Investigator).
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Phase:
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N/A
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Countries of recruitment
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Lebanon
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Contacts
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Name:
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Zoher Naja, MD |
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Address:
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Telephone:
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+9611636000 |
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Email:
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zouhnaja@yahoo.com |
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Affiliation:
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Name:
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Zoher Naja, MD |
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Address:
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Telephone:
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Email:
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zouhnaja@yahoo.com |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- elective unilateral herniorrhaphy
Exclusion Criteria:
- history of allergic reactions to local anesthetics
- bleeding diatheses
- spinal abnormality
Age minimum:
2 Months
Age maximum:
7 Years
Gender:
Male
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Health Condition(s) or Problem(s) studied
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Reduce Pain After Herniorrhaphy
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Intervention(s)
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Other: Anesthesia induction
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Other: PVB injection at L1-L2
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Other: PVB injections at T12-L1, L1-L2 and L2-L3.
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Primary Outcome(s)
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Analgesic consumption
[Time Frame: 24 hours postoperatively]
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Secondary Outcome(s)
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Hemodynamic stability
[Time Frame: During the operation (approximately one hour)]
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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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