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Clinical case control of 200 cases of insomnia treated with Mongolian medicine Sugemule-4

Clinical study on the treatment of insomnia with Mongolian medicine compound Sugemule-4 and characterization of its pharmacological substances and mechanism of action - Mongolian medicine Sugemule-4

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091100
Enrollment
Unknown
Registered
2024-10-21
Start date
2023-02-27
Completion date
Unknown
Last updated
2024-10-28

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

Conditions

insomnia

Interventions

experimental group:The experimental group was treated with Mongolian medicine Sugemule-4
control group:The control group was treated with estazolam

Sponsors

The Fourth People's Hospital of Ordos City
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients clinically diagnosed with insomnia (evaluated by the PSQI scale), Asens scale (AIS), abnormal auditory evoked potential tests, abnormal sleep monitoring tests, and patients with clinical diagnostic elements of insomnia) 2. Clear consciousness and ability to understand language 3. Age over 18 years old and able to cooperate with treatment 4. Meets the diagnostic criteria for insomnia in CCMD-2-R.

Exclusion criteria

Exclusion criteria: 1. Individuals with a history of Mongolian medicine allergy. 2. Unclear and unable to cooperate with treatment 3. Patients with abnormal liver function and organic lesions in the middle stage of insomnia due to long-term insomnia 4. Breastfeeding, pregnant women.

Design outcomes

Primary

MeasureTime frame
Athens Insomnia Scale;Pittsburgh sleep quality index;Near infrared brain functional imaging;Auditory evoked test;sleep monitoring;

Countries

China

Contacts

Public ContactSun Lidong

The Fourth People's Hospital of Ordos City

935194526@qq.com+86 139 0477 2080

Outcome results

None listed

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