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Completed

NCT Number: NCT02708966

Effect of Gymnema Sylvestre on Patients With Impaired Glucose Tolerance.

Prediabetes (PD) was defined as an state in which glucose levels are above normal but not enough to meet criteria for the diagnosis of type 2 diabetes (T2D). PD can be presented as impaired fasting glucose (IFG), impaired glucose tolerance (IGT) and glycated hemoglobin A1c (A1C) altered. The International Diabetes Federation (IDF) reported that in 2013 the prevalence of IGT was 6.9% which is equivalent to approximately 316 million individuals with IGT, it is expected that by 2035 this number will increase to 417 million people affected. Many hypoglycemic effects attributed to Gymnema sylvestre have been reported, including: increase of insulin secretion, regeneration of pancreatic islet cells, increased glucose utilization in various ways and inhibition of glucose uptake in the intestine.

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Key information

Age range

30 year–59 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Institute of Experimental and Clinical Therapeutics (INTEC), CUCS, University of Guadalajara

Guadalajara, Jalisco, 44340, Mexico

About this study

The target is to evaluate the effect of the administration of Gymnema Sylvestre on glycemic control, insulin secretion and insulin sensibility on patients with IGT. The investigators will conduct a double-blind trial, randomized, placebo control group, each group 12 female and male patients, between 30 and 59 years old with IGT (2-h values in the oral glucose tolerance test, OGTT) from 140 mg / dL to 199 mg / dL), Body Mass Index (BMI) from 25 to 34.9 kg / m2. Randomization will determine who will receive the intervention during the 9-week trial (Gymnema Sylvestre capsules, 300 mg 2 times daily with the first bite of breakfast and dinner or homologated placebo capsules). The clinical findings and laboratory tests include a metabolic profile and biosafety, which will be made at baseline and at week 9. Body weight, body fat, BMI and blood pressure will be determined during the initial and final visit. Adverse events and adherence to treatment will be documented. Statistical analysis: Mann-Whitney U test, Wilcoxon and Fisher exact test. It is considered with significance at p <0.05.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • BMI: 25.0-34.99 kg / m2.
  • Diagnosis of IGT (2h-OGTT Values between 140mg / dl and 199mg / dl.)
  • Written informed consent.
  • body weight stable over the last 3 months.
  • Women in follicular phase of the menstrual cycle (days 3 to 8 of the cycle) at the time of laboratory tests.
  • Women who are not contemplated get pregnant within the next 6 months.

Exclusion criteria

  • Women pregnant or breastfeeding.
  • Physical or mental disability that makes it impossible to perform the intervention.
  • Diagnosis of hypertension or heart failure.
  • Smokers.
  • Untreated thyroid disease.
  • Consumption of oral agents or other medications or supplements with proven properties that modify the behavior of glucose and lipids (oral hypoglycemic agents, insulin, lipid-lowering).
  • Diagnosis of liver disease or elevation twice of the upper normal value of liver enzymes.
  • Diagnosis of renal disease or creatinine > 1.5 mg / dl.
  • Diagnosis of Type 2 Diabetes Mellitus (T2DM) Fasting glucose ≥ 126 mg / dL and/or 2h-OGTT ≥ 200 mg / dL and/or A1C ≥ 6.5%.
  • Total Cholesterol ≥ 280 mg/dL.
  • Triglycerides ≥ 300 mg/dL.
  • Known allergy to calcined magnesia or Gymnema sylvestre.

Treatment and study plan

Gymnema Sylvestre

Drug

Gymnema Sylvestre, 300mg capsules 2 times daily with the first bite of breakfast and dinner

Other names: Gurmar

Placebo

Drug

Placebo, 300mg capsules 2 times daily with the first bite of breakfast and dinner

Other names: Calcined Magnesia

Primary outcomes

  1. Fasting Plasma Glucose

    Time frame: 90 days

    After intervention by spectrophotometry

  2. 2-hour Post Load Plasma Glucose (2-h PG)

    Time frame: 90 days

    The blood sample for determining of 2-h PG, was taken two hours after the ingestion of the drink with 75 g dextrose and was evaluated by spectrophotometry method. The value was expressed on mmol/L.

  3. Glycated Hemoglobin A1c (A1C)

    Time frame: 90 days

    After intervention by high-performance liquid chromatography

  4. Total Insulin Secretion (Insulinogenic Index)

    Time frame: 90 days

    Total insulin secretion was calculated with the insulinogenic index (ΔABC insulin / ΔABC glucose) after intervention.

  5. First Phase of Insulin Secretion

    Time frame: 90 days

    First phase of insulin secretion was estimated using the Stumvoll index (1283+ 1.829 x insulin 30' - 138.7 x glucose 30' + 3.772 x insulin 0') after intervention.

  6. Insulin Sensitivity (Matsuda Index)

    Time frame: 90 days

    Insulin sensitivity was calculated with Matsuda index [10,000 / √glucose 0' x insulin 0') (mean glucose oral glucose tolerance test (OGTT) x mean insulin OGTT)] after intervention.

Secondary outcomes

  1. Area Under the Curve of Glucose

    Time frame: 90 days

    Area under the curve of glucose was obtained using the trapezoidal integration.

  2. Area Under the Curve of Insulin

    Time frame: 90 days

    After intervention area under the curve of insulin

  3. Body Weight (BW)

    Time frame: 12 weeks

    The weight was measured at baseline, week 4, week 8 and week 12 with a bioimpedance balance and the entered values reflect the weight at week 12

  4. Body Mass Index (BMI)

    Time frame: 12 weeks

    The Body Mass index was calculated at baseline and at week 12 with the Quetelet index and the entered values reflect the body mass index at week 12

  5. Waist Circumference (WC)

    Time frame: 12 weeks

    Waist circumference was evaluated at baseline and at week 12 with a flexible tape and the entered values reflects the waist circumference measure at week 12

  6. Systolic Blood Pressure (SBP)

    Time frame: 12 weeks

    The Systolic Blood Pressure was evaluated at baseline and week 12 with a digital sphygmomanometer and the entered values reflect the blood pressure at week 12

  7. Diastolic Blood Pressure (DBP)

    Time frame: 12 weeks

    The Diastolic blood pressure was evaluated at baseline and week 12 with a digital sphygmomanometer and the entered values reflect the blood pressure at week 12

  8. Total Cholesterol

    Time frame: 90 days

    After intervention by spectrophotometry

  9. Triglycerides

    Time frame: 90 days

    After intervention by spectrophotometry

  10. High Density Lipoprotein Cholesterol

    Time frame: 90 days

    After intervention by spectrophotometry

  11. Low Density Lipoprotein

    Time frame: 90 days

    After intervention by spectrophotometry

  12. Very Low Density Lipoprotein

    Time frame: 90 days

    After intervention by spectrophotometry

  13. Creatinine

    Time frame: 90 days

    After intervention by spectrophotometry

Sponsors and collaborators

Lead sponsor

University of Guadalajara

Other

Registry information

Official study title

Effect of the Administration of Gymnema Sylvestre on Glycemic Control, Insulin Secretion and Insulin Sensitivity in Patients With Impaired Glucose Tolerance.

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
Mar 15, 2016
Registry last updated
Feb 2, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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