Nasturtium (Tropaeolum Majus L) Intake and Biochemical Parameters in Pre-diabetic Subjects in Bogota Colombia
Pre Diabetes
About this trial
This is an interventional prevention trial for Pre Diabetes focused on measuring Tropaeolum majus L.
Eligibility Criteria
Inclusion Criteria:
- Patients aged 25-60 years, with a clinical diagnosis of glucose intolerance for at least six months.
- Body mass index (BMI) > 30 kg/m2. The BMI will be restricted to > 30 kg/m2 to reduce the variability in the lipid profile parameters, which frequently are normal in subject with normal BMI.
- Sign informed consent
Exclusion Criteria:
- Severe impairment of cardiac, hepatic or renal function.
- Gestation or lactation
- Use of insulin injection
- Pharmacotherapy with metformin or iDPP4, which alter insulin sensitivity or Glycaemia
- Consumption of antioxidant or vitamin supplements
- Consumption of estrogen or vitamin K-antagonists
Sites / Locations
- Hospital Universitario San Ignacio
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Nasturtium (NT)
Placebo (PLC)
5g freeze-dried nasturtium leaf powder ; Each participant was supplemented with 15 grams of freeze-dried nasturtium leaf powder (NT) or placebo (PLC) per wk during 4 wk. Each participant received 3 envelopes per wk with 5 g NT each or 3 g PLC. In total each participant was given 24 envelopes (12 NT and 12 PLC) packaged in the same way to be indistinguishable from each other. The participants were instructed to take three days at wk one NT or PLC envelope diluted in 300 ml (about 10.14 oz) in chilly water in a bottle provided for the study
3g collagen colored with green pigment used in the food industry; Each participant was supplemented with 15 grams of freeze-dried nasturtium leaf powder (NT) or placebo (PLC) per wk during 4 wk. Each participant received 3 envelopes per wk with 5 g NT each or 3 g PLC. In total each participant was given 24 envelopes (12 NT and 12 PLC) packaged in the same way to be indistinguishable from each other. The participants were instructed to take three days at wk one NT or PLC envelope diluted in 300 ml (about 10.14 oz) in chilly water in a bottle provided for the study