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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05088733
Other study ID # BJDHYZY
Secondary ID
Status Recruiting
Phase Early Phase 1
First received
Last updated
Start date July 1, 2020
Est. completion date June 30, 2023

Study information

Verified date November 2021
Source Beijing Ditan Hospital
Contact Zhiyun Yang, doctor
Phone +8613439696988
Email 13439696988@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Clinical research of Yang Yin Fu Zheng Jie Du therapy in HBV related hepatocellular carcinoma induced anemia. The purpose of this study is to observe the efficacy of routine medical care combined with Yang Yin Fu Zheng Jie Du therapy for patients belong to HBV-HCC induced anemia.


Recruitment information / eligibility

Status Recruiting
Enrollment 120
Est. completion date June 30, 2023
Est. primary completion date June 30, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Meet the criteria of hepatocellular carcinoma - Patients who tested positive for hepatitis B surface antigen (HBsAg) for >6 months - Meet the criteria of anemia - Ages Eligible for Study: =75 years old; - Informed consent from the patient. Exclusion Criteria: - Patients with upper gastrointestinal bleeding within 3 months before enrollment; - History of blood transfusion within 3 months before enrollment; - Patient with other chronic hepatopathy, such as AIH, NAFLD, ALD; - Serious problem of heart, lung, or kidney with severe dysfunction; - Pregnant or child breast feeding women; - Mental or cognitive disorders; - Participating in other drug trials; - Who are allergic to the study drug.

Study Design


Intervention

Drug:
Yang Yin Fu Zheng Jie Du therapy
Yang Yin Fu Zheng Jie Du is a Chinese herbal compound.
Other:
Routine medical care
Routine medical care

Locations

Country Name City State
China Zhiyun Yang Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Beijing Ditan Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Survival rate 1 year
Secondary Objective response rate 1 year
Secondary quality of life (QOL) questionnaire The questionnaire includes appetite, sleep, fatigue, pain, etc. 1 year
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