Skip to content

A clinical study for treatment of type 2 diabetes with Fuhuang Jiangze capsule

A clinical study for treatment of type 2 diabetes with Fuhuang Jiangze capsule

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021765
Enrollment
Unknown
Registered
2019-03-08
Start date
2019-04-01
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

Type 2 diabetes(Qi yin two deficiency heat syndrome)

Interventions

Experimental group:Huang Huang drops sugar capsules, 6 tablets each time, 3 times a day, half an hour before the meal. Metformin hydrochloride tablets: The original daily dose remains unchanged, oral.
Control group:Simulated yellow sugar capsules, 6 at a time, 3 times a day, half an hour before the meal. Metformin hydrochloride tablets: The original daily dose remains unchanged, oral.

Sponsors

First Affiliated Hospital of Xiamen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years, gender is not limited; 2. Patients with type 2 diabetes who meet the criteria for Western diagnosis of diabetes; 3. In line with the Chinese medicine Qi Yin two false heat syndrome; 4. Only treated with dimethyl diguanidine hydrochloride, and the dose is stable, not less than 4 weeks; 5. Poor control: Blood sugar[ 6.5 mmol/L = FPG(venous blood) = 10.0 mmol/L; 7.0 % HbA1c(glycated hemoglobin) = 8.0 %(based on the detection value of each center)]; 6. Subjects were informed and voluntarily signed an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Type 1 diabetes, gestational diabetes, type 2 diabetes and other special types of diabetes requiring insulin treatment; 2. Patients with acute complications of diabetes; 3. Combine serious heart and cerebrovascular diseases and serious primary diseases such as liver, kidney and hematopoietic system; 4. Allergies and allergies to known ingredients of drugs; 5. Pregnant and lactating women and those who have recent birth plans; 6. Long-term alcohol abuse, drug dependence, and mental illness; 7. Patients treated with oral Chinese medicine or proprietary Chinese medicine within 1 month before screening; 8. Those who had participated or were participating in clinical trials of other drugs within one month prior to the screening period of this study; 9. The researchers considered it inappropriate to participate in this clinical researcher.

Design outcomes

Primary

MeasureTime frame
Changes in the treatment of hemoglobin glycosylated during the 12th weekend compared to the baseline period;

Secondary

MeasureTime frame
Changes in fasting and postprandial 2H blood sugar per visit point;Treatment of changes in islet function in the 12th weekend compared to the baseline period(insulin release test, area under curve, insulin resistance index);Treatment of Chinese medicine syndrome on the 12th weekend compared with the baseline changes in curative effect;Quality of Life Scale for Treatment of Diabetes at the 12th Weekend;Symptoms, signs, disappearance, or clinical control.;

Countries

China

Contacts

Public ContactYang shuyu

Xiamen University Affiliated First Hospital

xdfyec@sina.com+86 13950062003

Outcome results

None listed

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