TENS in Scleroderma

Recruiting Phase 1 Interventional Study
Scleroderma Gastroparesis Systemic Sclerosis (SSc)
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Device Feasibility
Participants needed
16 (estimated)
Sponsor
University of Michigan · Other
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About This Trial
The goal of this pilot study is to assess the acceptability of the transcutaneous electrical acustimulation (TEA) device in treating Scleroderma-related gastroparesis. The main objective is: To evaluate the acceptability of TEA as an intervention for alleviating symptoms of distension and bloating in individuals diagnosed with Scleroderma. Participants will be provided with the TEA devices that …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Classification of Systemic Sclerosis according to the 2013 American College of Rheumatology and European League against Rheumatism classification criteria. 2. Age \>= 18 years 3. English speaking. 4. Participants who report moderate to severe symptoms of distension/bloatin…
Contacts

Dinesh Khanna, MD, MSc

734-936-5615

khannad@med.umich.edu

CONTACT