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The Effects of Trichosanthes Root on Blood Sugar in Patients With Diabetes Mellitus

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02855645
Enrollment
60
Registered
2016-08-04
Start date
2016-07-31
Completion date
Unknown
Last updated
2016-11-16

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

Conditions

Diabetes Mellitus

Keywords

Trichosanthes root, Traditional Chinese Medicine, Clinical trial

Brief summary

Diabetes mellitus (DM) locates fifth of ten leading death etiology, the population of diabetic patients has a tendency of increase. Trichosanthes root is called as Tian Hua Fen, According to traditional Chinese writing record that Trichosanthes root has the action of downbear fire, moisten dryness, and slippery phlegm, and release thirst. The Trichosanthes root may lower blood sugar levels in the modern study. The investigators designed a double blind, randomized controlled study, a total of 60 diabetic patients with high blood sugar were divided into treatment and control groups, and each group was 30 patients. In the treatment group, oral administration of Trichosanthes root 1.5 g, bid/day for 84 days continuously; in the control group, oral administration of Trichosanthes root placebo 1.5 g, bid/day for 84 days continuously. The main outcome measure was the changes of plasma blood sugar and Glycated hemoglobin A1c (HbA1c) levels changed before and after Trichosanthes root treatment. The investigators predict the results of the present study indicated that Trichosanthes root can improve plasma blood sugar and glycated hemoglobin A1c levels.

Interventions

DRUGTrichosanthes root

Trichosanthes root at a rate of 1.5 g two times per day for 84 days.

DRUGPlacebo

Trichosanthes root at a rate of 0.15g (10%) two times per day for 84 days.

Sponsors

China Medical University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Early diagnosis Type Ⅱ Diabetic patients who Glycated hemoglobin A1c level between 7.0% and 9.0% (including) , and after three months of diet and exercise control. 2. The subject who was taking hypoglycemic drugs Metformin, the maximum total amount of ≦ 1500 mg / day. 3. Age ranged between 20 and 80 years (including).

Exclusion criteria

1. Pregnancy or breast-finding. 2. Allergy to test medicine. 3. Type I Diabetic patients. 4. Bleeding tendency. 5. The participants who suffered from serious disorders, such as congestive heart failure, myocardial infarction, chronic obstructive pulmonary disease, renal failure, cancer or stroke etc. 6. Irritable or anxious patients who cannot be assessed. 7. Refuse to sign the agreement. 8. The values of SGOT and SGPT levels were more than normal limit triple, or the value of creatinine level was more than normal limit. 9. Plasm glucose(Glucose AC) level in fasting state ≧ 300 mg / dL.

Design outcomes

Primary

MeasureTime frameDescription
Glycated hemoglobin A1cThree monthsImprovement of glycated hemoglobin A1c levels
Plasma Blood SugarThree monthsImprovement of Plasma Blood Sugar levels

Countries

Taiwan

Contacts

Primary ContactChing-Liang Hsieh, M.D., Ph.D
clhsieh@mail.cmuh.org.tw+886-4-22053366

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026