DiCART TM Device for Capillary Refill Time Measurement (DICART-VS)

Civil Hospices of Lyon logo

Civil Hospices of Lyon

Status

Completed

Conditions

Peripheral Perfusion

Treatments

Device: measure capillary refill time

Study type

Interventional

Funder types

Other

Identifiers

NCT04538612
69HCL18_0217
2019-A00094-53 (Other Identifier)

Details and patient eligibility

About

To estimate peripheral perfusion in shock state, international guidelines recommend the use of capillary refill time, and practitioners currently evaluates it at bedside. However its measurement is not standardized, what should explain the large observer variability reported in different studies. Hence, a device providing a standardized evaluation seems to be helpful. The aim of the study is to evaluate diagnostic performance of such a device recently developped (DiCART TM), in healthy volunteers experiencing vascular occlusion tests to induce impaired perfusion.

Enrollment

20 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy volunteers
  • Age > 18 years old
  • Informed consent to participate

Exclusion criteria

  • Vascular disease
  • Diabetes mellitus
  • Dermatosis
  • Cutaneous lesion on a measurement site
  • Anemia
  • Pregnancy
  • Cardiovascular chronic treatment
  • Non affiliation to a social security regime
  • Involvement in other interventional study

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

measure capillary refill time
Experimental group
Treatment:
Device: measure capillary refill time

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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