Actively Recruiting
Microneurographic Assessment of Peripheral Nerves in Healthy Volunteers and Individuals With Sensory Dysfunction Caused by Inherited Mutations in the PIEZO2 Gene
Led by National Center for Complementary and Integrative Health (NCCIH) · Updated on 2026-05-14
16
Participants Needed
1
Research Sites
32 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Microneurographic Assessment of Peripheral Nerves in Healthy Volunteers and Individuals With Sensory Dysfunction Caused by Inherited Mutations in the PIEZO2 Gene
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Willing to comply with all study procedures and available for the study duration
- Male or female, aged 18 years and over
- Able to provide written informed consent
- Enrolled in protocol 16-AT-0077, "Clinical and Scientific Assessment of Pain and Painful Disorders"
- For PDS patients: Clinical and genetic diagnosis of PIEZO2 loss of function
- For healthy participants: In good general health as confirmed by medical evaluation under protocol 16-AT-0077
You will not qualify if you...
- Difficulty communicating that prevents reliable pain and sensation assessments
- Unable to comply with study procedures or visits
- Dermatological conditions that affect skin sensitivity
- Congenital limb deficiency or amputation of any limb
- History of fainting (syncope)
- Peripheral neuropathy or chronic pain conditions in the past year, including treatment with neuropathic pain medications
- Major medical conditions like kidney, liver, heart, neurological, or chronic systemic diseases including diabetes or Raynaud's Disease
- Untreated mental health conditions such as depression, bipolar disorder, psychosis, anxiety, or substance use disorders
- Pregnant or breastfeeding
- Participation in other research that interferes with sensation studies
- Employee or staff at NCCIH
- Adults unable to provide their own consent
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
National Institutes of Health Clinical Center
Bethesda, Maryland, United States, 20892
Actively Recruiting
Research Team
H
Hayley M Hansen
CONTACT
M
Miroslav Backonja, M.D.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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