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A multicenter real world study to evaluate the efficacy of Niuhuangqingxin Pill in the treatment of Insomnia, depressive disorder, bipolar disorder, somatoform disorder, epilepsy, stroke convalescence, post-stroke cognitive impairment, hypertension, coronary heart disease

A multicenter real world study to evaluate the efficacy of Niuhuangqingxin Pill in the treatment of Insomnia, depressive disorder, bipolar disorder, somatoform disorder, epilepsy, stroke convalescence, post-stroke cognitive impairment, hypertension, coronary heart disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100053404
Enrollment
Unknown
Registered
2021-11-20
Start date
2021-11-18
Completion date
Unknown
Last updated
2022-09-26

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

Conditions

Insomnia, depressive disorder, bipolar disorder, somatoform disorder, epilepsy, stroke convalescence, post-stroke cognitive impairment, hypertension, coronary heart disease

Interventions

insomnia group:Niuhuangqingxin Pill
depressive disorder group:Niuhuangqingxin Pill
bipolar disorder group:Niuhuangqingxin Pill
somatoform disorder group:Niuhuangqingxin Pill
epilepsy group:Niuhuangqingxin Pill
stroke group:Niuhuangqingxin Pill
hypertension group:Niuhuangqingxin Pill
coronary heart disease group:Niuhuangqingxin Pill

Sponsors

Guangdong Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients meet the diagnosis criteria of one of the following disease: insomnia, depressive disorder, bipolar disorder, somatoform disorder, epilepsy, stroke convalescence, post-stroke cognitive impairment, hypertension, coronary heart disease, including course of treatment and drug combination; 2.Patients who are taking Niuhuangqingxin Pill; 3.Patients who provided voluntary written consent to take part in this study.

Exclusion criteria

Exclusion criteria: 1. Those who are allergic to (administration) Niuhuang Qingxin Pill and its components, or are allergic; 2. Women who are pregnant, planning to become pregnant or breastfeeding; 3. Those who are participating in another clinical trial; 4. The investigator judges that it is not suitable to participate in this trial.

Design outcomes

Primary

MeasureTime frame
Insomnia severity Index scale;Hamilton rating scale for depression;young manic rating scale;Health Questionnaire-15;the National Institutes of Health Stroke Scale;Mini-Mental State Examination;Seattle Angina Questionnaire;Seizure frequency(1month);blood pressure;TCM syndrome integral scale;

Countries

China

Contacts

Public ContactJia Fujun

Guangdong Provincial People's Hospital

jiafujun@126.com+86 13609049731

Outcome results

None listed

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