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Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up during the surgery
Awards & highlights
Study Summary
This trial will compare a new nerve stimulator to the standard one to see if it's better for pediatric patients during surgery.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ during the surgery
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~during the surgery
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
EMG changes
Trial Design
1Treatment groups
Experimental Treatment
Group I: TetragraphExperimental Treatment1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Tetragraph (TM) NMT Monitor
2021
N/A
~100
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Who is running the clinical trial?
Joseph D. TobiasLead Sponsor
20 Previous Clinical Trials
3,704 Total Patients Enrolled
4 Trials studying Surgery
382 Patients Enrolled for Surgery
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You weigh between 44 - 132 pounds.You have swelling in your body tissues.You have a history of a nerve disorder outside of the brain and spinal cord.You are unable to use your arm for blood pressure monitoring.
Research Study Groups:
This trial has the following groups:- Group 1: Tetragraph
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.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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