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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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19 February 2015 |
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Main ID: |
NCT02237326 |
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Date of registration:
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03/09/2014 |
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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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Visual Inspection With Acetic Acid Compared to Lugol's Iodine in HIV-infected Women
SAVE |
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Scientific title:
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Safety and Validity Evaluation for Cervical Cancer Screening and Treatment Techniques Among HIV-infected Women |
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Date of first enrolment:
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October 2011 |
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Target sample size:
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654 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT02237326 |
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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, Masking: Single Blind (Caregiver), Primary Purpose: Diagnostic
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Phase:
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N/A
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Countries of recruitment
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Kenya
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- 23-59
- Intact cervix/uterus
- no evidence of infection
- ability to provide informed consent
Exclusion Criteria:
- pregnant
Age minimum:
23 Years
Age maximum:
59 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Cervical Intraepithelial Neoplasia
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Cervical Cancer
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HIV
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Intervention(s)
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Procedure: Visual Inspection with Acetic Acid
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Procedure: Visual Inspection with Lugol's Iodine
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Primary Outcome(s)
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Test Positivity Rate
[Time Frame: eight months]
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Secondary Outcome(s)
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Sensitivity
[Time Frame: 12 Months]
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Secondary ID(s)
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10-00197
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SSC 1825
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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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