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Clinical evaluation of swallowing assistive gel in assisting capsule swallowing for post-stroke patients

Clinical evaluation of swallowing assistive gel in assisting capsule swallowing for post-stroke patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016636
Enrollment
Unknown
Registered
2018-06-14
Start date
2018-06-15
Completion date
Unknown
Last updated
2018-06-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Interventions

Stroke group:swallowing assistive gel
Compare group:swallowing assistive gel

Sponsors

The Third Affiliated Hospital of Sun Yat-Sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Clinically diagnosed as hemorrhagic or ischemic stroke; 2. Functional oral intake scale(FOIS) level 4-7; 3. No aspiration or choking in water swallowing test; 4. Agreed to participate in the study and signed an informed consent.

Exclusion criteria

Exclusion criteria: 1. Individuals with organic diseases as tumor, malformation and etc in swallowing related organs; 2. Individuals who cannot participate in VFSS; 3. Disagreed to participate in the study.

Design outcomes

Primary

MeasureTime frame
Successful rate of capsule swallowing;—

Secondary

MeasureTime frame
qualitative parameters of VFSS;—

Countries

China

Contacts

Public ContactZulin Dou

The Third Affiliated Hospital of Sun Yat-Sen University

douzul@163.com+86 18922102718

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026