Skip to content

Study on cerebral infarction (acute phase) complicated with obstructive sleep apnea hypopnea syndrome screening and oropharyngeal muscle exercise (training)

Study on cerebral infarction (acute phase) complicated with obstructive sleep apnea hypopnea syndrome screening and oropharyngeal muscle exercise (training)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000038312
Enrollment
Unknown
Registered
2020-09-17
Start date
2019-11-01
Completion date
Unknown
Last updated
2020-12-14

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

Conditions

Cerebral infarction(acute phase) complicated with obstructive sleep apnea hypopnea syndrome

Interventions

not complicated with SAHS group VS mild SAHS group VS moderate SAHS group VS severe SAHS group:No intervention measures taken. Conduct data analysis.
Patients taking orofacial myofunctional therapy:No intervention measures taken. Conduct self before-after study

Sponsors

The First Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who meet all criteria can be included as experimental cases 1. Meet the requirements of diagnostic criteria for acute cerebral infarction. 2. The disease did not progress within 24 hours. 3. 18-85 years old. 4. Sign informed consent, agree to accept all kinds of treatment methods (portable polysomnography screening, etc.) in this study.

Exclusion criteria

Exclusion criteria: Patients who meet any of the following should be excluded 1. Patients with serious disturbance of consciousness and unable to cooperate with the examination. 2. Supplementary oxygen, positive airway pressure, mechanical ventilation or gastric tube should be used. 3. Progressive or other serious central nervous system diseases, serious sleep disorders other than sleep apnea, neuromuscular diseases, hypoxemia caused by other medical conditions. 4. Progressive or life-threatening diseases. 5. Pregnancy.

Design outcomes

Primary

MeasureTime frame
Polysomnography;TCM syndrome factors scale of ischemic stroke;

Secondary

MeasureTime frame
NIHSS scale;Mini-mental State Examination;The Epworth Sleeping Scale;Stanford Sleepiness Scale;STOP-BANG questionnaire;The cooperation and activation of patients and their accompanies to exercise the orofacial myofunctional therapy;

Countries

China

Contacts

Public ContactYu Zhengmiao Guo Wei

The First Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine

yuzhengmiao@yeah.net+86 13710633518

Outcome results

None listed

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