Concordance of Capillary Blood Biological Samples With Conventional Venousbiological Blood Samples. (CAPIVEIN)
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| ClinicalTrials.gov Identifier: NCT03890146 |
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Recruitment Status :
Terminated
(we submitted an amendment. The study was stopped because this amendment raised the complexity of the study.)
First Posted : March 26, 2019
Last Update Posted : January 29, 2021
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| Condition or disease |
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| Biochemical Dysfunction |
The completion of a biological test suits a succession of codified steps:
- Medical prescription
- The pre-analytic phase (preparation of the material, completion of the sample, transport of the sample and preparation of it)
- The analytical phase
- The post-analytic phase (validation of the result obtained and the dissemination of it to the prescriber, usually the clinician, who is then able to make a medical decision) This succession of steps involves, as part of a classical journey, many stakeholders (doctors, nurses, couriers, laboratory technicians, medical biologists) in different places.
Outsourced biology (care test point, POCT) refers to the analysis of biological samples outside the central laboratory. The sample is most often carried out, transported and analyzed by the same person on a machine near the patient or in the service and therefore in the absence of direct control of a specialized laboratory technician or a medical biologist, who remains however responsible for good practice, maintenance of the device and validity of the results.
The completion of biological examinations is regulated by differents Articles. The outsourced biology (ADBD) sampling analysis can be carried out in the hospital, in most departments, and also outside the hospital (pharmacies, city offices or even in the patient's own home). On portable devices, usually highly specialized, and these fixed allowing a greater diversity of tests.
Its development is booming with annual growth estimated in 2006 at 15.5% in the United States.
| Study Type : | Observational |
| Actual Enrollment : | 1 participants |
| Observational Model: | Cohort |
| Time Perspective: | Prospective |
| Official Title: | Concordance of Capillary Blood Biological Samples Analyzed in Delocalized Biology With Conventional Venous Biological Blood Samples Analyzed at the Biology Laboratory |
| Actual Study Start Date : | December 20, 2018 |
| Actual Primary Completion Date : | December 20, 2020 |
| Actual Study Completion Date : | December 21, 2020 |
| Group/Cohort |
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intensive care patients
patient hospitalised in intensive care unit veinous and capillary ponction
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- concordance between capillary and veinous sampling for natremia result [ Time Frame: 1 hour ]The concordance between the biological results obtained by capillary puncture analysed on the GEM 4000 resuscitation machine (Werfen), and the biological results by venous sampling analysed in the standard biology laboratory on the Gen. 2 COBAS machine (Roche) for natremia
- concordance between capillary and veinous sampling for kalemia result [ Time Frame: 1 hour ]The concordance between the biological results obtained by capillary puncture analysed on the GEM 4000 resuscitation machine (Werfen), and the biological results by venous sampling analysed in the standard biology laboratory on the Gen. 2 COBAS machine (Roche) for kalemia
- concordance between capillary and veinous sampling for chloremiaresult [ Time Frame: 1 hour ]The concordance between the biological results obtained by capillary puncture analysed on the GEM 4000 resuscitation machine (Werfen), and the biological results by venous sampling analysed in the standard biology laboratory on the Gen. 2 COBAS machine (Roche) for chloremia
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| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Patient over the age of 18
- Affiliate or beneficiary of a social security scheme
- Express consent to participate in the study
Exclusion Criteria:
- Patient benefiting from a legal protection measure
- Patient not communicating
- Pregnant or breastfeeding woman
- Peripheral edema (taking more than 5 Kg since entering the service)
- Patient in shock (mean arterial pressure < 65 mmHg or continuous catecholamine administration)
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03890146
| France | |
| France | |
| Paris, France, 75019 | |
| Principal Investigator: | Nefeli Nasika | Fonadtion Afolphe Rothschild |
| Responsible Party: | Fondation Ophtalmologique Adolphe de Rothschild |
| ClinicalTrials.gov Identifier: | NCT03890146 |
| Other Study ID Numbers: |
2018-A01880-55 |
| First Posted: | March 26, 2019 Key Record Dates |
| Last Update Posted: | January 29, 2021 |
| Last Verified: | January 2021 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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intensive care capillary sampling veinous sampling |
natremia kalaemia Chloremia |

