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Clinical efficacy and safety of compound Lingzhi Anshen oral liquid in the treatment of convalescent patients with coronary heart disease

Clinical efficacy and safety of compound Lingzhi Anshen oral liquid in the treatment of convalescent patients with coronary heart disease

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091481
Enrollment
Unknown
Registered
2024-10-29
Start date
2023-02-12
Completion date
Unknown
Last updated
2024-11-04

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

Conditions

novel coronavirus infection

Interventions

Treatment group:Oral compound Lingzhi Anshen oral liquid + routine treatment
Control Group:routine treatment

Sponsors

Taizhou Enze Medical Center (Group) Enze Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. The convalescent patients with Covid-19 infection; 2. Aged 18-85 years old (including the cut-off value) , and the sex was not limited; 3. The patients accepted the treatment voluntarily and signed the informed consent. 4. BFI score >= 4 or Athens insomnia scale score >= 7

Exclusion criteria

Exclusion criteria: 1. The patients whose condition is not stable, 2. The patients whose consciousness is not clear, who have disturbance of consciousness, dementia, who can not understand the contents of the scale and check up and all kinds of psychosis, 3. The pregnant and lactating women; Women of childbearing age who were unable or unwilling to use adequate contraception during the trial or their spouses who were unwilling to use contraception; 4. Patients receiving oral or injection of Erythropoietin, hypnotic drugs, melatonin, or other Chinese patent medicines (pcms) 5. Patients who are participating in clinical trials of other drugs, and who are known to be allergic to therapeutic drugs; 6. The researcher judges that the patient is not suitable to participate in the study according to the clinical situation.

Design outcomes

Primary

MeasureTime frame
fatigue;sleep quality;

Secondary

MeasureTime frame
life of quality ;Hemoglobin;Interleukin-6;

Countries

China

Contacts

Public ContactXiaomai Wu

Taizhou Enze Medical Center (Group) Enze Hospital

Wuxm@enzemed.com+86 139 5856 6762

Outcome results

None listed

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