MedTrace Logo

Optimal Blood Sampling Site for Point of Care Lactate Assessment

NCT04291989 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2020-03-02

No results posted yet for this study

Summary

The study was to compare blood Lactate levels between ear lobe and finger against venous forearm blood sample using the electronic hand held lactate device in hip fracture patients with good cognitive function (AMT \>/= 7)

Conditions

  • Blood Lactic Acid Increased
  • Hip Fractures

Interventions

DEVICE

Optimal Blood Sampling Site for Point of Care Lactate Assessment using the handled Lactate-Pro 2 device

This study aims to compare lactate levels using the Lactate Pro 2 device from the same patient at the same time with blood samples taken from three locations - fingertip, earlobe and forearm venepuncture

Sponsors & Collaborators

  • University Hospitals, Leicester

    lead OTHER

Principal Investigators

  • GANAPATHY RAMAN R Perianayagam, FRCS (Orth) · University Hospitals, Leicester

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-07-18
Primary Completion
2019-03-20
Completion
2019-03-20

Countries

  • United Kingdom

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04291989 on ClinicalTrials.gov