An Examination of Blinding for Chinese Herbal Oral Liquid and Matched Placebo

Guangzhou University of Traditional Chinese Medicine

Status: Completed

Conditions: Placebo Evaluate

Treatments: Drug: Chinese herbal medicine FYTF-919

Study type: Interventional

Funder types: Other

Identifiers

NCT05483595

BE2022-187

Details and patient eligibility

About

TCM is an essential context of the ICH management in Chinese culture. Given the potential benefits of Chinese herbal medicine Zhongfengxingnao formula (ZFXN) in reducing haematoma and bleeding after acute intracerebral hemorrhage (ICH) from fundamental research and small clinical studies, more reliable evidence is required to guide ICH treatment using TCM. This study is designed to evaluate the blinding and physical consistency between the investigational drug and placebo in RCT, taking the trial named Chinese herbal medicine in patients with acute intracerebral hemorrhage (CHAIN) as an example. Therefore the blinding of placebo as well as and physical consistency with investigated TCM in CHAIN trial will be determined. In addition, an assessment method for blinding and physical consistency could be developed for subsequent placebo evaluations.

Full description

A total of 48 subjects will be divided into two parts for manual scoring, which includes not only the proportion of the discrimination to ZFXN, which is the primary outcome in this study, but also the physical (odor, taste) consistency of the two drugs. The primary outcome was the percentage of ZFXN response. The secondary outcomes included artificial sensory score and intelligent sensory attributes of testing drug.

Enrollment: 48 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• 1. Age ≥18 years old;
• 2. No visual, olfactory, taste, cognitive impairment;
• 3. Provide written informed consent by patient (or approved surrogate);

Exclusion criteria

• 1. Evaluation personnel involved in the clinical trial about ZFXN;
• 2. Subjects with severe history of heart, liver, kidney, digestive tract, nervous system, respiratory system, mental disorders or metabolic disorders;
• 3. Subject with history of food, drug allergies, or other allergic diseases (asthma, urticaria, eczematous dermatitis, etc.) or is known to be allergic toZFXN;
• 4. Known definite contraindication to the Chinese herbal medicine;
• 5. Women who are known to be pregnant or lactating;
• 6. Subjects not fit to participate in this study judged by responsible treating clinician.

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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48 participants in 2 patient groups

ZFXN group

Other group

Description:

Subjects actually testing ZFXN

Treatment:

Drug: Chinese herbal medicine FYTF-919

Placebo group

Other group

Description:

Subjects actually testing placebo

Treatment:

Drug: Chinese herbal medicine FYTF-919