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Showing 1-4 of 4 trials for Postural-orthostatic-tachycardia-syndrome-pots
Recruiting

Study of Natriuretic Peptide Receptor 1 (NPR1) Antagonist in Adult Patients With Postural Orthostatic Tachycardia Syndrome (POTS)

Arizona · Gilbert, AZ

This study is researching an experimental drug called REGN7544 (called "study drug"). The study is focused on participants with POTS. The aim of the study is to see how safe, tolerable, and effective the study drug is. The study is looking at several other research questions, including: * How the study drug changes heart rate and blood pressure in participants with POTS * What side effects may happen from taking the study drug * How much study drug is in the blood at different times * Whether the body makes antibodies against the study drug (which could make the study drug less effective or could lead to side effects)

Recruiting

Phenotyping of Postural Orthostatic Tachycardia Syndrome (POTS)

Texas · Dallas, TX

This is an observational study to deeply phenotype the disorder of POTS using multiple testing modalities.

Recruiting

Programming Aquatic Therapy for POTS

Long Beach, California

The goal of this pilot study is to create, implement, and evaluate an aquatic therapy for Postural Orthostatic Tachycardia Syndrome (POTS) program feasibility and ability to improve quality of life as determined by reduced orthostatic tachycardia, reduced POTS symptoms, and improved quality of life measures. The main questions it aims to answer are: Does aquatic occupational therapy reduce orthostatic tachycardia and POTS symptoms? Does aquatic occupational therapy lead to higher quality of live measures for people with POTS? Is this aquatic occupational therapy program feasible for clinicians and people with POTS? There is no comparison group for this pilot study. Participants will complete: An occupational Therapy evaluation before and after program completion (3 hours total) 30 minutes at home/remote 30 minutes on-site/in-person 30 minutes of individualized occupational therapy on land Participate in 3 aquatic therapy sessions per week, 60 minutes each for 12 weeks

Recruiting

Long COVID Cutaneous Signatures: An ARPA Funded Research Project

Arizona · Scottsdale, AZ

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.