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Technical Standardization and Clinical Evaluation Research of Shallow Needle Therapy for Chronic Insomnia

Technical Standardization and Clinical Evaluation Research of Shallow Needle Therapy for Chronic Insomnia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000409
Enrollment
Unknown
Registered
2024-09-10
Start date
2023-08-23
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

chronic insomnia

Interventions

Experimental Group:(1)1mg of dzopicone orally once daily
(2)shallow needles therapy once daily and five times a week.
Control Group:1mg of dzopicone orally once daily.

Sponsors

The Affiliated People's Hospital of Fujian University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) patients who met the diagnostic criteria; (2) insomnia patients aged 18 to 65 years; (3) Pittsburgh Sleep Quality Index (PSQI) score:7~15; (4) the duration of the disease = 3 months (5) no communication and cognitive impairment; (6) voluntary enrollment and signed informed consent.

Exclusion criteria

Exclusion criteria: (1) secondary insomnia; (2) those who do not wish to undergo shallow needles therapy; (3) pregnant or lactating women or those who intend to become pregnant; (4) combined with heart liver kidney lung brain and other serious organic diseases; (5) participants in other studies that influenced the results of this study.

Design outcomes

Primary

MeasureTime frame
Pittsburgh sleep quality index;

Secondary

MeasureTime frame
Magnetic resonance spectroscopy of the thalamus;Sleep structure;Insomnia severity index;Hamilton anxiety scale;To determine the serum levels of melatonin dopamine norepinephrine;

Countries

China

Contacts

Public ContactWanqing Lin

The Affiliated People's Hospital of Fujian University of Traditional Chinese Medicine

13960829639@139.com+86 139 6082 9639

Outcome results

None listed

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