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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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28 June 2021 |
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Main ID: |
NCT02671656 |
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Date of registration:
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29/01/2016 |
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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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Study of the Reliability of a Device (HumanSens Plus) Allowing Immediate Measurement Uric Acid in the Blood Obtained by Finger Tip Puncture.
URICA |
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Scientific title:
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Reliability Assessment of the HumaSens Plus Measurement of Uricemia in Capillary Blood |
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Date of first enrolment:
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March 2016 |
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Target sample size:
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0 |
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Recruitment status: |
Withdrawn |
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URL:
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https://clinicaltrials.gov/show/NCT02671656 |
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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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France
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Contacts
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Name:
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Thomas BARDIN, MD, PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Assistance Publique - Hôpitaux de Paris |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Patients seen in the diabetology day hospital
- Patients aged at least 18 years-old
- French-speaking patients
- Patients able to understand the study and the information form
Exclusion Criteria:
- Patients unable to understand the aim of study aind the information sheet
- Patients not affiliated to a social security scheme (beneficiary or assignee)
Age minimum:
18 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Diabetes
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Intervention(s)
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Device: Uricemia
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Primary Outcome(s)
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Uricemia
[Time Frame: Day0]
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Secondary Outcome(s)
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Uricemia on capillary blood vs on serum
[Time Frame: Day0]
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Haematocrit, glucose and lipid levels, medications
[Time Frame: Day0]
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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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