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A prospective case series study of obstructive sleep apnea in the treatment of adjusting of physique and spirit

A prospective case series study of obstructive sleep apnea in the treatment of adjusting of physique and spirit

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104590
Enrollment
Unknown
Registered
2025-06-19
Start date
2023-08-17
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Obstructive sleep apnea

Interventions

Treatment group:Acupuncture

Sponsors

Dongzhimen Hospital, Beijing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1: Age 18-65 years old, both sexes 2: Meet the diagnostic criteria for OSA; 3: Meet the traditional Chinese medicine diagnostic criteria of snoring 4: Subjects were informed consent.

Exclusion criteria

Exclusion criteria: 1: The patients were diagnosed as central or mixed sleep apnea, and the proportion of mixed or central sleep apnea was =50% 2: Have received any other form of OSA treatment or participated in other clinical trials within the past 3 months 3: With severe nasal septum deviation, nasal polyps, nasal tumors, pharyngeal cancer, mandibular retraction, small micromaxillary deformity or other significant craniofacial anomalies may affect breathing 4: With severe heart, brain, lung, liver, kidney, nerve and hematopoietic system disease, malignant tumor, mental illness and cognitive impairment 5: A positive pregnancy test, who are pregnant or breastfeeding, and who have recently planned to have children 6: Severe fear of acupuncture or faintng during acupuncture treatment, unable to adhere to complete the treatment 7: Known or suspected history of allergy to study devices and materials 8: A suspected or real history of alcohol or drug abuse or dependence 9: The researchers think that is not suitable to participate in this clinical study.

Design outcomes

Primary

MeasureTime frame
Apnea - Hypopnea Index, AHI;

Secondary

MeasureTime frame
Modified Mallampati Score;Epworth Sleepiness Scale;Neck circumference;Self-rating anxiety scale;Self-rating depression scale;LSaO2;body weight and BMI;

Countries

China

Contacts

Public ContactJinxia NI

Dongzhimen Hospital, Beijing University of Chinese Medicine

ziniuzhang@126.com+86 84013161

Outcome results

None listed

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