Skip to content

Clinical Observation on the treatment of Obstructive sleep apnea syndrome by needle-knife release of anterior cervical fascia

Clinical Observation on the treatment of Obstructive sleep apnea syndrome by needle-knife release of anterior cervical fascia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117053
Enrollment
Unknown
Registered
2026-01-19
Start date
2026-01-19
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Obstructive sleep apnea syndrome

Interventions

Control group:Control group: Basic internal medicine treatment: Under the condition of actively controlling blood pressure, blood sugar, blood lipid, etc., drugs that improve cerebral circulation and
Treatment group:Treatment group: On the basis of the treatment in the control group, needle-knife treatment was added twice a week.

Sponsors

Beijing Hospital of Integrated Traditional Chinese and Western Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)Age: 18 to 70 years old; Both men and women are welcome. (2) Obstructive sleep apnea confirmed by PSG or qualified out-of-hospital testing, with AHI >= 15 times per hour. (3) Those who can receive needle-knife treatment. (4) No treatment for other diseases related to this disease was received in the half month prior to this treatment. (5) Good compliance with treatment, willing to accept follow-up and complete the treatment. (6) Be informed of the trial and sign the informed consent form

Exclusion criteria

Exclusion criteria: Those who have known allergies or intolerance to needle-knife treatment (such as severe coagulation disorders, uncontrolled local infections, etc.). (2) The main type is central sleep apnea (with central events accounting for more than 50%). (3) Those who have undergone relevant neck surgeries recently (within 6 months) or have obvious anatomical abnormalities in the neck and require surgical intervention. (4) Those with severe heart, liver or kidney insufficiency, active infections, severe mental disorders or those who are unable to cooperate. (5) Pregnant or lactating women. (6) Situations where other researchers consider it inappropriate to participate in this study. Patients who cannot complete or refuse to fill out the scale or refuse to participate in PSG.

Design outcomes

Primary

MeasureTime frame
Apnea-hypopnea index;

Countries

China

Contacts

Public ContactXiaoleiWu

Beijing Hospital of Integrated Traditional Chinese and Western Medicine

208899195@qq.com+86 135 8198 4912

Outcome results

None listed

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