New swallowing test could spot hidden risks in SMA patients
NCT ID NCT04773470
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This completed study looked at how well a camera test called FEES (flexible endoscopic evaluation of swallowing) can detect and track swallowing problems in people with spinal muscular atrophy (SMA). Researchers studied 79 SMA patients of different types and ages, using several standard scales to measure swallowing safety and function. The goal was to improve diagnosis and monitoring of dysphagia, which is common in SMA and can lead to serious complications.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to better, standardized ways to detect and monitor swallowing problems in SMA, helping guide treatment decisions.
- What could go wrong
- This is a completed diagnostic study, not a treatment trial. The findings may not change clinical practice immediately and need further validation.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
79 people
The number who actually took part.
- Started
-
Feb 2022
- Finished
-
Sep 2024
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: All patients with genetically determined 5q-linked SMA followed at the neuromuscular center Gießen \- Informed and written consent signed by the patient or a legal guardian Exclusion Criteria: * Physical illness that, according to its type and severity, could interfere with the planned assessments, could have an influence on the parameters to be investigated or could endanger the patient or test person during the course of the investigation. * Pregnancy or lactation and a positive pregnancy test * Acute suicidal tendency or external danger * Poor general condition
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Spinal muscular atrophy are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
University Hospital Giessen and Marburg, Campus Giessen
Giessen, Hesse, 35392, Germany
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can more Hands-On therapy and home devices help children with SMA?
- Can a brain implant let paralyzed people control computers with their minds?
- Can treating spinal muscular atrophy in the womb be safe and helpful? a new registry aims to find out
- A Baby's fidgets may reveal brain health: study tests early warning signs
- Can a muscle-boosting antibody help people with spinal muscular atrophy over the long haul?
- Can a patient registry unlock the secrets of spinal muscular atrophy?