CClinicalTrials.gg
Status unknownNCT02902848COAGHEMOUpdated Sep 16, 2016

Evaluation of the Validity of the Prothrombin Time Internation Normalised Ratio (PT/INR) Measured at the point-of Care on the Arterial Bloodline of Haemodialysis Extracorporeal Blood Flow

An observational study in Haemodialysis, sponsored by University Hospital, Brest. Status unknown at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2016-09-16.

Sponsored by University Hospital, Brest · Observational

The sponsor has not verified this record recently (last verified Sep 2016), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
30
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to evaluate the INR value of hemodialyzed patient coagulation state (prothrombin time) measured inside the therapeutical zone and thanks to a portable monitor. The values obtained at the point of care will be compared to the standard biological assessment.

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Conditions studied

  • Haemodialysis
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In context

Lead sponsor

University Hospital, Brest is the lead sponsor of 594 studies on the registry; 135 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The population of the study is the patients under haemodialysis treatment, who need INR monitoring

Eligibility criteria

Inclusion Criteria:

  • Age > 18
  • Haemodialyzed patient whose INR needs to be monitored
  • Patient not objecting to participate in the study
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
30 participants (estimated)
Patient registry
No
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What researchers measure

Primary outcomes

  1. correlation ratio between point-of-care PT/INR value and standard laboratory assessement

    Time frame: 5 months

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Study locations

1 of 1 sites recruiting
  • CHU Brest
    Brest, 29200, France
    Recruiting
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 16, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02902848
Lead sponsor
University Hospital, Brest
Responsible party
Sponsor
First posted
Sep 16, 2016
Start date
Mar 2015
Primary completion
Mar 2017 (estimated)
Last update
Sep 16, 2016

Study contacts

Yannick Le meur, MD-PhD
Contact
yannick.lemeur@chu-brest.fr
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Sep 2016. You cannot join it, but the record below documents what was studied.

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