StrokeNCT06615310
Ultrasonographic Parameters in Stroke Patients With Dysphagia
An observational study of Stroke and Dysphagia, run by Istanbul Physical Medicine Rehabilitation Training and Research Hospital at 1 site in Turkey (Türkiye).
Trial summary
ultrasonographic parameters in stroke patients with dysphagia Read more about this study
- Who is it for?
- Any age
- What is being tested?
- ultrasonograpic evaluotion
- How many people
- 52 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 1 Feb 2025to 1 Feb 2026
- How long will I take part?
- 1 Day
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: Patients who have been diagnosed with stroke at Istanbul Physical Therapy and Rehabilitation Training and Research Hospital and enrolled in a rehabilitation program will be divided into 2 groups according to the presence of dysphagia (3 points and above according to the EAT-10 scale).
Who may be able to join
- Agreeing to participate in the study,
- Cognitive competence to understand the test instructions
- Communication skills to respond to the test instructions.
Who cannot join
- Presence of a neurological disease other than stroke that will cause difficulty in swallowing, -Being illiterate,
- refusing to participate in the study,
- jaw joint problem,
- surgical intervention in the neck area that will affect ultrasound measurements,
- infected open wound
Trial locations and contacts
1 site in 1 country.
Turkey (Türkiye)1 site
Istanbul Fizik Tedavi ve Rehabilitasyon Eğitim ve Araştırma Hastanesi
Istanbul
About this study
Official title: The Relationship of Ultrasonographic Parameters Used in the Evaluation of Dysphagia in Stroke Patients With Swallowing Severity
ultrasonographic parameters in stroke patients with dysphagia
- Being tested
- ultrasonograpic evaluotion
- Medical subject headings
- Stroke, Deglutition Disorders
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ultrasonograpic evaluotionOther
The distance between the hyoid and thyroid cartilage, the volume of the geniohyoid, digastric anterior, sternohyoid and thyrohyoid muscles will be evaluated by ultrasound.
| Study group | Role | What they receive |
|---|---|---|
| dysphagia | 3 Points and above according to the EAT-10 scale Receives: Other: ultrasonograpic evaluotion | |
| non-dysphagia | Under 3 points on the EAT-10 scale Receives: Other: ultrasonograpic evaluotion |
What is being measured
The primary outcome is the main question the study is designed to answer.
muscle volume of thyrohyoid
the thickness of the muscle will be measured by ultrasound
Measured: baseline
Secondary outcomes (1)
muscle volume of sternohyoid
the thickness of the muscle will be measured by ultrasound
Measured: baseline
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 Sep 2024
- Study start1 Feb 2025
- Primary completion1 Oct 2025
- Study completion1 Feb 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for StrokeStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case-control
- Time perspective
- Prospective
- Enrolment
- 52 participants (actual)
- Target duration
- 1 Day
Sponsor and investigators
- Lead sponsor
- Istanbul Physical Medicine Rehabilitation Training and Research Hospital
- Sponsor type
- Other government
- Responsible party
- Principal investigator, Cansin Medin, Istanbul Physical Medicine Rehabilitation Training and Research Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06615310
- Sponsor's protocol ID
- 2024-41
- Status last verified
- Jun 2026
- First submitted
- 13 Sep 2024
- Last updated
- 18 Jun 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 18 Jun 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Relationship of Ultrasonographic Parameters Used in the Evaluation of Dysphagia in Stroke Patients With Swallowing Severity
- ClinicalTrials.gov ID
- NCT06615310
- Acronym / sponsor ID
- 2024-41
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 52 participants (actual)
- Lead sponsor
- Istanbul Physical Medicine Rehabilitation Training and Research HospitalOther government
- Study start
- 1 Feb 2025 (actual)
- Primary completion
- 1 Oct 2025 (actual)
- Study completion
- 1 Feb 2026 (actual)
- First posted
- 26 Sep 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
ultrasonographic parameters in stroke patients with dysphagia
Study design
- Observational model
- Case-control
- Time perspective
- Prospective
- Target follow-up
- 1 Day
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| dysphagia | – | Other: ultrasonograpic evaluotion3 Points and above according to the EAT-10 scale |
| non-dysphagia | – | Other: ultrasonograpic evaluotionUnder 3 points on the EAT-10 scale |
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Patients who have been diagnosed with stroke at Istanbul Physical Therapy and Rehabilitation Training and Research Hospital and enrolled in a rehabilitation program will be divided into 2 groups according to the presence of dysphagia (3 points and above according to the EAT-10 scale).
Key inclusion criteria (3 listed)
- Agreeing to participate in the study,
- Cognitive competence to understand the test instructions
- Communication skills to respond to the test instructions.
Key exclusion criteria (5 listed)
- Presence of a neurological disease other than stroke that will cause difficulty in swallowing, -Being illiterate,
- refusing to participate in the study,
- jaw joint problem,
- surgical intervention in the neck area that will affect ultrasound measurements,
- infected open wound
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| ultrasonograpic evaluotionThe distance between the hyoid and thyroid cartilage, the volume of the geniohyoid, digastric anterior, sternohyoid and thyrohyoid muscles will be evaluated by ultrasound. | Other | dysphagia, non-dysphagia |
Primary outcome
muscle volume of thyrohyoid
Time frame: baseline
the thickness of the muscle will be measured by ultrasound
1 secondary outcome
muscle volume of sternohyoid
Time frame: baseline
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 Jun 2026.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Stroke and Dysphagia, run by Istanbul Physical Medicine Rehabilitation Training and Research Hospital at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 18 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
muscle volume of thyrohyoid (time frame: baseline). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Jun 2026.