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Clinical study on the treatment of patients with insomnia characterized by irritability using Zhichi Suanzaoren Decoction

Clinical study on the treatment of patients with insomnia characterized by irritability using Zhichi Suanzaoren Decoction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000705
Enrollment
Unknown
Registered
2024-11-13
Start date
2024-12-01
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

insomnia

Interventions

treatment group:Zhichi Suanzaoren Decoction

Sponsors

Hangzhou Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Meeting the aforementioned diagnostic criteria; 2. Aged between 18 and 65 years; 3. First episode of illness with a duration of =3 months; 4. The patient is conscious and stable in vital signs; 5. Scoring >56 on the Novaco Anger Inventory Scale and voluntarily participating in the entire treatment process and having signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Suffering from mental or psychological disorders; 2. Having taken medication or health products that can improve sleep or may affect sleep within 2 weeks prior to enrollment; 3. Having weakened immune function; 4. Pregnant or breastfeeding women; 5. Unable to take traditional Chinese medicine; 6. Participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Novaco Anger Inventory;STAXI-2;Traditional Chinese Medicine Syndrome Score Scale;Pittsburgh sleep quality indexs;Insomnia Severity Index;

Countries

China

Contacts

Public ContactZHANG Yonghua

Hangzhou Traditional Chinese Medicine Hospital

zyh16916@163.com13306510088

Outcome results

None listed

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