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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: |
NCT03544710 |
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Date of registration:
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20/05/2018 |
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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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Impact of Preoperative Bathing on Post Caesarean Section Surgical Site Infection
SSI-MUST |
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Scientific title:
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The Impact of Preoperative Bathing With Chloroxylenol on the Incidence of Post Caesarean Section Surgical Site Infection at Mbarara Regional Referral Hospital: A Randomized Controlled Trial |
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Date of first enrolment:
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December 7, 2017 |
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Target sample size:
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96 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03544710 |
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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: Prevention. Masking: Single (Outcomes Assessor).
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Phase:
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N/A
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Countries of recruitment
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Uganda
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Contacts
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Name:
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Henry Lukabwe, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Mbarara University of Science and Technology |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- All mother scheduled for delivery by emergency C/S at MRRH during the study period.
Exclusion Criteria:
- Women who declined to consent.
- Women with obvious evidence of infection, like fever, foul-smelling liquor, or those
already on antibiotics for reasons other than preoperative prophylaxis.
- Women in whom delivery was indicated to occur within less than 30 minutes, like in
fetal distress, obstructed labor, pulsatile cord prolapse, or ruptured uterus.
- Women who could not communicate and give information for the study and those who do
not have a working telephone contact.
Age minimum:
15 Years
Age maximum:
49 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Cesarean Wound Disruption With Postnatal Complication
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Intervention(s)
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Other: preoperative bathing with antiseptic
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Primary Outcome(s)
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Surgical site infection
[Time Frame: 30 days]
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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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