Skip to content

Effect of Gynostemma Pentaphyllum Tea in Insulin Sensitivity in Type 2 Diabetic Patients

Gynostemma Pentaphyllum Tea Improves Insulin Sensitivity in Type 2 Diabetic Patients

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01254084
Enrollment
16
Registered
2010-12-06
Start date
2010-02-28
Completion date
2010-11-30
Last updated
2010-12-06

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

Conditions

Type 2 Diabetes

Keywords

Herbal medicine; Type 2 diabetes; Gynostemma pentaphyllum Tea; Insulin sensitivity;

Brief summary

The aim of the present study was to investigate the effects of Gynostemma Pentaphyllum tea on insulin sensitivity in drug-naïve type 2 diabetic patients.

Detailed description

In Vietnam, traditional herbal medicines have played a major role in the management of diabetes for centuries. Gynostemma Pentaphyllum (GP) Makino (Family Cucurbitaceae) is a perennial creeping herb growing wild in the mountainous regions of Vietnam, China and some other Asian countries and was widely used in Southeast Asian countries as an herbal medicine and being beneficial for the prevention and treatment of diabetes. We have previously published the evidences that GP tea possessed anti-diabetic effect with good safety data in newly diagnosed T2D patients, and had effect on insulin sensitivity. In addition extract of GP had been shown to reduce both hyperglycemia and hyperlipidemia in diabetic Zucker Fatty rats. So the present study was to investigate the effects of Gynostemma Pentaphyllum tea in insulin sensitivity in type 2 diabetic patients.

Interventions

DIETARY_SUPPLEMENTGynostemma Pentaphyllum tea

6g/day per oral, twice a day in 10 weeks, 30 minutes before breakfast and dinner

DIETARY_SUPPLEMENTPlacebo tea

6g/day per oral, twice a day in 10 weeks, 30 minutes before breakfast and dinner

Sponsors

Karolinska Institutet
CollaboratorOTHER
Swedish International Development Cooperation Agency (SIDA)
CollaboratorOTHER_GOV
Hanoi Medical University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
40 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Newly diagnosed, drug-naive patients with type 2 diabetes * Fasting plasma glucose: 7-11 mmol/l * HbA1C: 7-9%.

Exclusion criteria

* Type 1 diabetes * Liver and kidney failure

Design outcomes

Primary

MeasureTime frameDescription
Fating plasma glucose, Steady state plasma glucose in Somatostatin-Insulin-Glucose Infusion Test10 weeksAll subjects participated in Somatostatin-Insulin-Glucose Infusion Test (SIGIT), lasting 150 minutes, performed at 8am after an 8-10h overnight fast with only tap water allowed ad libitum. Somatostatin was used to suppress endogenous insulin release, thereby allowing estimation of sensitivity to exogenously administered insulin by measuring blood glucose value at 90, 120 and 150 minute of the test (SIGIT mean).

Secondary

MeasureTime frame
Liver enzymes (ALT, AST)10 weeks
Kidney function (S-creatinine, S-BUN)10 weeks
Plasma lipids (TG, Cholesterol, HDL-, LDL-)10 weeks
Blood pressure10 weeks
Body weight (BMI, hip-waist ratio)10 weeks

Countries

Vietnam

Outcome results

None listed

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