Reference Range Analysis of the Entegrion Point of Care Coagulation Monitor (PCM™) in Healthy Volunteers
NCT03133351 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 240
Last updated 2020-04-16
Summary
This study is intended to define the PCM normal laboratory range.
Conditions
- Coagulation
Interventions
- DEVICE
-
PCM
A fresh whole blood sample will be tested by PCM to determine the reference range.
Sponsors & Collaborators
-
Entegrion, Inc.
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2017-04-04
- Primary Completion
- 2020-12-30
- Completion
- 2021-03-31
- FDA Device
- Yes
Countries
- United States
Study Locations
More Related Trials
-
Evaluation of Physiological Variables and Detection of Blood Loss in Healthy Adults With Different Subject Positioning by the CM-1500
NCT05980013 ·Status: COMPLETED ·Phase: NA
-
A Study to Obtain Additional Information on the Use of CorMatrix® CanGaroo ECM® Envelope
NCT02418143 ·Status: WITHDRAWN
-
Procalcitonin Test Reference Range Determination
NCT02591121 ·Status: COMPLETED
-
Evaluation of the Zynex Blood Volume Monitor in Healthy Adult Patients During a Blood Draw
NCT01846195 ·Status: COMPLETED ·Phase: NA
-
Clinical Performance of the Investigational GEM Hemochron® 100 in Populations Ages 18 Years and Older
NCT03074266 ·Status: UNKNOWN
-
Evaluation of the Zynex Blood Volume Monitor in Healthy Adult Volunteers During a Blood Draw
NCT01834612 ·Status: COMPLETED ·Phase: PHASE1
-
Normal Reference Range Study With the TEG6s Heparin Neutralization Cartridge in Healthy Volunteers
NCT06261580 ·Status: COMPLETED
-
QStat Pilot Reference Range Study
NCT04490759 ·Status: COMPLETED
-
Reference Range Study for the Quantra QStat System
NCT04219371 ·Status: COMPLETED
-
Clinical Evaluation of the OEC Elite Vascular Mobile Fluoroscopy System
NCT03096483 ·Status: TERMINATED ·Phase: NA
-
Evaluation of the Clinical Performance of the Quantra System With the Quantra Surgical Cartridge
NCT03152461 ·Status: COMPLETED
-
Assessment of a Diagnostic Medical Device for the INR (International Normalized Ratio) Measurement
NCT02779400 ·Status: COMPLETED ·Phase: NA
-
Home Usage of Conception Kit Instructions
NCT00326651 ·Status: UNKNOWN
-
HemoSphere Alta Study
NCT07148323 ·Status: RECRUITING
-
Evaluate Retention of an Orally Administered Device Using Gamma Scintigraphy Study 2
NCT00780286 ·Status: COMPLETED ·Phase: PHASE1
-
Comparison Study for Bioelectrical Impedance Device to Measure Human Body Composition
NCT00956917 ·Status: COMPLETED ·Phase: NA
-
Clinical Evaluation of the Zynex Blood Volume Monitor (CM-1500) in Healthy Male Adult Subjects During a Blood Draw
NCT01646060 ·Status: COMPLETED ·Phase: PHASE1
-
Comparison of Bioimpedance Body Composition Device Measurements
NCT01888068 ·Status: COMPLETED
-
Implementing Myocardial Computed Tomographic Perfusion in a Community Hospital Setting
NCT02756234 ·Status: COMPLETED
-
Evaluation of a Novel Method of Contrast Volume Quantification - AVERT PLUS 2.0
NCT02578173 ·Status: COMPLETED
-
Evaluation of Physiological Variables and Detection of Blood Loss Using the Zynex Fluid Monitoring System, Model CM-1600
NCT05463198 ·Status: COMPLETED ·Phase: NA
-
Trima Accel® System Post Count Algorithm Study
NCT02684630 ·Status: COMPLETED ·Phase: NA
-
Evaluation of Accuracy and Consistency of the X-Trodes System
NCT05722639 ·Status: COMPLETED
-
Evaluation of the Accuracy of the Hemochron Signature Elite Point of Care Device Compared With Laboratory Assay
NCT02255214 ·Status: COMPLETED
-
Survey of Tourniquet Use in a Combat Support Hospital
NCT00517166 ·Status: COMPLETED