NT-3 Levels and Function in Individuals With CMT

Peripheral Neuropathy Clinical Trial

Official title:

Correlation of Circulating NT-3 Levels and Function in Individuals With Peripheral Neuropathy or Charcot-Marie-Tooth Neuropathy

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05011006
• Other study ID #: 19-0353
• Status: Recruiting
• Start date: November 13, 2019
• Est. completion date: June 2024

Study information

• Verified date: March 2023
• Source: Nationwide Children's Hospital
• Contact: Dawn Scott, RN
• Phone: 614722-2715
• Email: Dawn.Scott[@]nationwidechildrens.org
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This study will assess the serum NT-3 levels in individuals with the diagnosis of peripheral neuropathy or any type of Charcot-Marie-Tooth Neuropathy (CMT) and correlate this with function.

Description:

This study will assess the serum NT-3 levels in those with a peripheral neuropathy diagnosis which will help to determine the therapeutic levels of NT-3 in subjects that will receive AAV1.NT-3 gene therapy in a future study. This study also aims to define the natural history of any type of Charcot-Marie Tooth Disease (CMT), better define the rate of disease progression and skeletal muscle involvement. Another aim is to generate a registry of well-characterized CMT patients who may be candidates for future trials.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 50
• Est. completion date: June 2024
• Est. primary completion date: June 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 7 Years and older

Eligibility

Inclusion Criteria:

• Males or females from 7 years of age or older

• Diagnosis of acquired peripheral neuropathy (PN) such as due to diabetes, chemo-induced, autoimmune chronic inflammatory demyelinating polyneuropathy (CIDP) established by a report of electrical studies or with a known genetic CMT diagnosis. Definitive diagnosis of PN is established with a report of electrical studies, EMG/nerve conduction studies.2

• Perform assessments to the best of their ability with reliable results as deemed by the evaluator.

• Ability to attend scheduled appointments

• Ability to provide informed consent (or assent for ages 9-18)

Exclusion Criteria:

• Current pregnancy per medical history

• Has a medical condition or extenuating circumstances that, in the opinion of the investigator, might compromise the subject's wellbeing, safety, or clinical interpretability

Related Conditions & MeSH terms

• Charcot-Marie-Tooth Disease
• Chronic Inflammatory Demyelinating Polyneuropathy
• Hereditary Sensory and Motor Neuropathy
• Nerve Compression Syndromes
• Peripheral Nervous System Diseases
• Peripheral Neuropathy
• Polyneuropathies
• Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
• Tooth Diseases

Intervention

Diagnostic Test:
• NT3 blood draw
blood draw

Locations

Country	Name	City	State
United States	Nationwide Children's Hospital	Columbus	Ohio

Sponsors (1)

Lead Sponsor	Collaborator
Zarife Sahenk

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Assess change in Manual Muscle Testing (MMT)	Weakness in the major motor groups can be documented by using manual muscle testing. This exam allows the symmetry of strength, along with distribution and degree of weakness to be assessed. The Medical Research Council lists the major motor groups as: neck flexion, hip extension, knee flexion, ankle plantar flexion, and hip abduction. Depending on the clinical circumstances, the exam can be individualized. The Medical Research Council provides a scale ranging from 0-5. Inter-rater reliability will be documented by all evaluators of the trial. A rating of 5 indicates full range of motion, whereas a rating of 0 indicates no movement.	Compare baseline to Year 1 and Year 2 visits.
Primary	Assess change in 100 Meter Timed Test (100m):	Directions for study procedures will be provided in a way the subject can understand (i.e. verbal and/or written instruction, demonstration, practice, etc.). Once the subject is comfortable with study procedures, they will complete the 100m test one time. Patients will be asked to run a set course of 25 meters for 4 laps for a total distance of 100 meters. The time to complete in seconds will be recorded.	Compare baseline to Year 1 and Year 2 visits.
Primary	Assess change in Timed Functional Testing:	Timed Functional Testing can include time to ascend/descend 4 standard-sized stairs, time to rise from the floor (from NSAD), and the 10-meter run (from the NSAD).	Compare baseline to Year 1 and Year 2 visits.
Primary	Assess change in PROMIS Upper Extremity Function and Mobility Scales:	The PROMIS Upper Extremity Function and Mobility instruments are patient-reported outcomes (PRO) that utilize a patient reported and/or parent proxy scale based on the patient's age that measures an individual's perceived upper extremity function and mobility.	Compare baseline to Year 1 and Year 2 visits.
Primary	Assess change in Abilities Captured Through Interactive Video Evaluation (ACTIVE)	ACTIVE is a video game that utilizes the Microsoft Kinect camera to measure functional reaching volume while the patient is motivated to squish spiders or collect gems.	Compare baseline to Year 1 and Year 2 visits.
Primary	Assess change in CMT Pediatric Scale (CMTPedS)	The CMTPedS is a clinician-administered scale that rates patient performance on various functional activities involving the upper extremities, lower extremities, balance, and gait. The CMTPedS generates a linear score of disability ranging from 0 (not affected) to 44 (severely affected).	Compare baseline to Year 1 and Year 2 visits.
Primary	Assess change in Timed Up and Go	The Timed Up and Go test (TUG) is a simple test used to assess a person's mobility and requires both static and dynamic balance. It uses the time that a person takes to rise from a chair, walk three meters, turn around, walk back to the chair, and sit down.	Compare baseline to Year 1 and Year 2 visits.
Primary	Assess change in Forced Vital Capacity	Forced expiratory volume (FEV) measures how much air a person can exhale during a forced breath. Forced vital capacity (FVC) is the total amount of air exhaled during the FEV test.	Compare baseline to Year 1 and Year 2 visits.
Primary	Assess change in Exploratory Gait Evaluation	We may attempt to quantify gait using vibration sensors, activity monitors, or a portable walkway providing temporal spatial gait analysis.	Compare baseline to Year 1 and Year 2 visits.