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: |
NCT03007927 |
Date of registration:
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20/12/2016 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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Evaluation of Dexamethasone Added to the Usual Infiltration With Bupivacaine in Inguinal Hernia Repair Mesh
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Scientific title:
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Evaluation of Dexamethasone Added to the Usual Infiltration With Bupivacaine in Inguinal Hernia Repair Mesh |
Date of first enrolment:
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August 2016 |
Target sample size:
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82 |
Recruitment status: |
Completed |
URL:
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https://clinicaltrials.gov/show/NCT03007927 |
Study type:
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Interventional |
Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Prevention. Masking: Double (Participant, Investigator).
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Phase:
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Phase 4
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Countries of recruitment
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Argentina
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Contacts
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Name:
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Sebastian SR Roche, doctor |
Address:
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Telephone:
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Email:
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Affiliation:
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Hospital Italiano de Buenos Aires |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
1. Patients older than 18 years.
2. Unilateral inguinal hernioplasty.
3. That the surgery is performed in the Ambulatory Surgery Unit (UCA).
Exclusion Criteria:
1. Recurrent hernia.
2. allergies, ongoing infections, diabetes.
3. Background of rejection of prosthetic material (mesh).
Age minimum:
18 Years
Age maximum:
75 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Pain, Postoperative
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Intervention(s)
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Drug: Bupivacaine- physiological solution
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Drug: Bupivacaine-Dexamethasone
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Primary Outcome(s)
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pain postoperative
[Time Frame: 3 month]
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Secondary Outcome(s)
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take analgesic
[Time Frame: 1 month]
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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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