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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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12 December 2020 |
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Main ID: |
NCT03392636 |
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Date of registration:
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08/12/2017 |
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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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Comparison of Recurrence Rate of 2 Herniotomy Techniques in Children Older Than 2 Years
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Scientific title:
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Comparison of Recurrence Rate of Ferguson & Gross Herniotomy With Mitchell Banks Herniotomy in Children Older Than 2 Years |
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Date of first enrolment:
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November 11, 2016 |
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Target sample size:
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260 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03392636 |
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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: Treatment. Masking: Triple (Participant, Care Provider, Outcomes Assessor).
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Phase:
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N/A
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Countries of recruitment
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Pakistan
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- All pediatric patients of either gender above age of 2 years and below 14 years of age
presenting in pediatric surgery Mayo hospital lahore
Exclusion Criteria:
- sliding hernia strangulated hernia pts with connective tissue disorders pts with
undesccended testis patients with hydrocele hernia with internal ring 2cm or more in
size
Age minimum:
2 Years
Age maximum:
13 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Hernia, Inguinal
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Intervention(s)
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Procedure: Herniotomy
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Primary Outcome(s)
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recurrence
[Time Frame: 6 months]
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Secondary Outcome(s)
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post-operative complications
[Time Frame: will be noted on follow up at 7 days post op]
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Testicular Atrophy
[Time Frame: 6 months after procedure]
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operation time
[Time Frame: upto 6 months, will be noted at the end of every procedure]
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size of incision
[Time Frame: upto 6 months, will be noted at the end of every procedure]
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Intra operative complications
[Time Frame: upto 6 months, will be noted at the end of every procedure]
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Secondary ID(s)
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212/RC/KEMU
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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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