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Lactate Sensor
Pilot Testing a Novel Non-invasive Lactate Sensor
N/A
Waitlist Available
Led By Peter E Light, PhD
Research Sponsored by University of Alberta
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
No Placebo-Only Group
Summary
This trial tests a new device called Lactisense that measures lactate levels through the skin without drawing blood. It targets people doing strenuous leg exercises because their lactate levels rise during such activities. The device uses microwaves to detect these changes and sends the data to a nearby reader.
Eligible Conditions
- Hyperlactatemia
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
That the lactate sensor under test is able track increase in interstitial lactate levels in exercising humans that follow the same time course as lactate values obtained from a commercial blood capillary lactate monitor.
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Evaluation of non-invasive lactate sensorExperimental Treatment1 Intervention
To determine the efficacy and accuracy of the non-invasive lactate sensor
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Lactate sensor (Lactisense)
2022
N/A
~10
Find a Location
Who is running the clinical trial?
University of AlbertaLead Sponsor
942 Previous Clinical Trials
434,400 Total Patients Enrolled
Peter E Light, PhDPrincipal InvestigatorUniversity of Alberta
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- Only people who are healthy and able to be physically active can participate.You have high blood pressure or a joint injury that would make it difficult for you to exercise.
Research Study Groups:
This trial has the following groups:- Group 1: Evaluation of non-invasive lactate sensor
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.