Microneurographic Assessment of Peripheral Nerves in Healthy Volunteers and Individuals With Sensory Dysfunction Caused by Inherited Mutations in the PIEZO2 Gene

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-100
SponsorNational Center for Complementary and Integrative Health (NCCIH)

About this trial

Background:

PIEZO2 Deficiency Syndrome (PDS) is a genetic disorder that affects a person s ability to feel touches and pain. Researchers want to know more about how PDS changes nerve function.

Objective:

To compare nerve function in people with PDS to that in people without PDS.

Eligibility:

People aged 18 years and older with PDS enrolled in protocol 16-AT-0077. Healthy volunteers are also needed.

Design:

Participants will have at least 1 clinic visit. They will undergo a test that measures activity in the nerves.

For the test:

Participants will place their arm or leg in a comfortable position.

Ultrasound will be used to locate nerves. A smooth wand will be slid over the skin to capture images of the structures below.

Two thin needles will be inserted through the skin. These needles are much smaller than the kind used to draw blood.

The needles will record nerve activity as different sensations are applied to the skin. These include mild electrical pulses; heat and cold; bending of the knee or elbow; vibration; air puffs; pulling a hair; and tapping, stroking (brushing), stretching, pinching, and pushing on the skin at different levels of force.

Each test takes 5 to 10 minutes. Participants will describe the sensations they feel.

Participants may opt for an additional test that measures how nerves respond after heat pulses are used to create mild redness on the skin.

Researchers would like at least 2 tests from each person. Participants may return for up to 3 additional visits, if desired, to complete all the testing.

Eligibility criteria

Qualifiers

Stated willingness to comply with all study procedures and availability for the duration of the study

Male or female, aged 18 years and over.

The ability to provide written informed consent.

Enrolled in 16-AT-0077, "Clinical and Scientific Assessment of Pain and Painful Disorders".

Disqualifiers

Difficulties with communication that make subjective innocuous and pain assessments impossible or unreliable.

Unable to comply with study procedures or visits.

Has a dermatological condition that might influence cutaneous sensitivity.

Congenital limb deficiency or amputation of any limb.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

16 Participants
are grouped into 2 trial groups