ClinicalTrials.Veeva

Menu

Deciphering Preserved Autonomic Function After Multiple Sclerosis (DPAF-MS)

Mayo Clinic logo

Mayo Clinic

Status

Enrolling

Conditions

Multiple Sclerosis
Autonomic Dysreflexia
Control Subjects

Treatments

Diagnostic Test: Tests of sympathetic activation
Diagnostic Test: Tests of sympathetic inhibition
Diagnostic Test: Testing of autonomic dysreflexia

Study type

Interventional

Funder types

Other

Identifiers

NCT07012135
24-007459

Details and patient eligibility

About

This study looks to characterize gradients of dysfunction in the autonomic nervous system in patients with clinically diagnosed multiple sclerosis. The autonomic nervous system plays key roles in regulation of blood pressure, skin blood flow, and bladder health- all issues that individuals with multiple sclerosis typically suffer. Focusing on blood pressure regulation, the most precise metric with broad clinical applicability, the investigators will perform laboratory-based tests to probe the body's ability to generate autonomic responses. For both individuals with multiple sclerosis and uninjured controls, laboratory-based experiments will utilize multiple parallel recordings to identify how the autonomic nervous system is able to inhibit and activate signals. The investigators anticipate that those with autonomic dysfunction with multiple sclerosis will exhibit abnormalities in these precise metrics. The investigators will look to see if any substantial connections exist between different degrees of preserved autonomic function and secondary autonomic complications from multiple sclerosis. In accomplishing this, the investigators hope to give scientists important insights to how the autonomic nervous system works after multiple sclerosis and give physicians better tools to manage these secondary autonomic complications.

Enrollment

13 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18-50 years old
  • clinically confirmed diagnosis of multiple sclerosis -OR- uninjured control

Exclusion criteria

  • symptoms of cardiovascular (including, but not limited to: hypertension, stroke, chest pain, etc.), respiratory, peripheral neurological or autonomic disease (particularly diabetes mellitus requiring treatment)
  • women who are pregnant or lactating
  • having a body mass index (BMI) ≥ 35 kg/m2
  • taking or being administered a medication known to potentially have adverse interactions with phenylephrine
  • in the judgement of the principal investigator or clinical collaborator, any illness or condition that will interfere with the patient's ability to comply with the protocol, compromise patient safety, or interfere with the interpretation of the study results

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

13 participants in 2 patient groups

Individuals with multiple sclerosis
Experimental group
Treatment:
Diagnostic Test: Testing of autonomic dysreflexia
Diagnostic Test: Tests of sympathetic inhibition
Diagnostic Test: Tests of sympathetic activation
Individuals without multiple sclerosis
Experimental group
Treatment:
Diagnostic Test: Testing of autonomic dysreflexia
Diagnostic Test: Tests of sympathetic inhibition
Diagnostic Test: Tests of sympathetic activation

Trial contacts and locations

1

Loading...

Central trial contact

Zachary Pohlkamp

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems