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Clinical Observation for the Effect of Wendan Decoction on Phlegm Syndrome Insomnia

Clinical Observation for the Effect of Wendan Decoction on Phlegm Syndrome Insomnia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900024942
Enrollment
Unknown
Registered
2019-08-04
Start date
2019-07-24
Completion date
Unknown
Last updated
2019-08-27

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

Conditions

Insomnia

Interventions

Sponsors

Department of Rehabilitation, Dongfang Hospital, Beijing University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1 Simultaneously conforms to the western medicine chronic insomnia diagnosis standard, Chinese medicine does not sleep diagnosis standard and the Chinese medicine phlegm syndrome diagnosis standard; 2 Aged 18 to 70 years; 3 Normal cognitive function.

Exclusion criteria

Exclusion criteria: 1 Patients with severe mental illness or anxiety or depression; 2 Drug dependence or alcohol dependence; 3 Pregnancy and lactation patients; 4 The survival period is less than 6 months; 5 Combined use of other traditional Chinese medicine preparations, lipid-lowering drugs or psychotropic drugs during treatment; 6 Use of lipid-lowering drugs within one month; 7 Hamilton anxiety scale score >= 14 or Hamilton depression scale (17 items) >=17. 8 Serious physical diseases.

Design outcomes

Primary

MeasureTime frame
Plasma melatonin;tg chohdlldl;

Countries

China

Contacts

Public ContactXing Jia

Dongfang Hospital of Beijing University of Traditional Chinese Medicine

dfyyxingjia@163.com+86 13810680063

Outcome results

None listed

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