Purpose

This is a prospective, longitudinal study involving 300 participants for a single visit to compare Long COVID neurocutaneous biosignatures with those of other disorders affecting the sensory and autonomic nervous system.

Conditions

Eligibility

Eligible Ages
Between 18 Years and 80 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  1. Long COVID defined by NIH PASC criteria OR 2. Acute COVID who tested positive for COVID without persistent symptoms OR 3. Postural orthostatic tachycardia syndrome (POTS) OR 4. Diabetic neuropathy

Exclusion Criteria

  1. Clinical evidence of severe peripheral vascular disease 2. History of ulceration, poor wound healing or vascular claudication 3. History of allergic reaction to local anesthesia (for biopsy collection) 4. Use of oral anticoagulants (aspirin or Plavix alone is allowed) 5. History of a bleeding disorder

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
Long COVID Participants with Long COVID
Acute COVID Participants with acute COVID who tested positive for COVID without persistent symptoms
Postural Orthostatic Tachycardia Syndrome (POTS) Participants with postural orthostatic tachycardia syndrome (POTS)
Diabetic neuropathy Participants with diabetic neuropathy

Recruiting Locations

CND Life Sciences
Scottsdale, Arizona 85258
Contact:
Aracely Galarza
4808470312
agalarza@cndlifesciences.com

More Details

NCT ID
NCT07005947
Status
Recruiting
Sponsor
CND Life Sciences

Study Contact

Aracely Galarza
480-434-6446
clinicalresearch@cndlifesciences.com

Detailed Description

This is a prospective, longitudinal study involving 300 participants for a single visit to compare Long COVID neurocutaneous biosignatures with those of other disorders affecting the sensory and autonomic nervous system. The evaluations will include clinical assessments, neurologic exams, patient reported outcome surveys, and skin biopsies from three locations. Data will be collected on the amount of P-SYN in cutaneous nerve fibers. The cohorts of interest are as follows: 1. 100 participants with Long COVID defined by NIH PASC criteria 2. 100 participants with acute COVID who tested positive for COVID without persistent symptoms defined WHO criteria 3. 50 participants with postural orthostatic tachycardia syndrome (POTS) 4. 50 participants with diabetic neuropathy There are no plans for additional visits at this time. If interested to learn more about this study, please complete the form here for someone to contact you. "here" would take you to the said form.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.