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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: |
NCT02611011 |
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Date of registration:
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18/11/2015 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Assessing the Usability and Clinical Utility of the Congo Red Dot Test: A Survey
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Scientific title:
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Assessing the Usability and Clinical Utility of the Congo Red Dot Test: A Survey |
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Date of first enrolment:
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March 1, 2018 |
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Target sample size:
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198 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02611011 |
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Study type:
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Observational |
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Study design:
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Phase:
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Countries of recruitment
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Mexico
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Contacts
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Name:
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Beverly Winikoff, Dr |
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Address:
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Telephone:
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Email:
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Affiliation:
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Gynuity Health Projects |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Eligible to consent for research
- Able to read Spanish well enough to read the test instructions
- Able to give informed consent
Exclusion Criteria:
- None
Age minimum:
10 Years
Age maximum:
50 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Preeclampsia
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Intervention(s)
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Device: Congo Red Test (GV-005)
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Primary Outcome(s)
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CRD Test Comprehension
[Time Frame: within 5 minutes of reading test instructions]
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Secondary Outcome(s)
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CRD Test Usability
[Time Frame: within 5 minutes of performing test]
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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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