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Evaluation of Cissus Verticillata L. Infusion in Controlling Type 2 Diabetes

Phase 1 Study for Testing Efficacy of Cissus Verticillata L Infusion in Controlling Glucose Concentration

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01145534
Enrollment
15
Registered
2010-06-16
Start date
2009-01-31
Completion date
2009-10-31
Last updated
2011-11-09

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

Conditions

Diabetes

Keywords

diabetes,, medicinal plants,, glucose

Brief summary

The purpose of this study was to investigate whether the infusion of a medicinal plant (Cissus verticillata L.) would be effective in reducing glucose levels in blood and saliva of type 2 Diabetes patients.

Detailed description

Type 2 diabetes mellitus is regarded as one of the most prevalent disease of the adult population. In many developing countries, this condition is regarded as major public health problem. Type 2 diabetes is a metabolic disorder characterized by high blood glucose related with a condition of insulin resistance and relative insulin deficiency. As Diabetes progresses, medications are necessary to control glucose levels. The aim of this study was to investigate whether the infusion of a medicinal plant (Cissus verticillata L.) would be as effective as a regular drug (glibenclamide) in reducing glucose levels in blood and saliva of type 2 Diabetes patients. Several medicinal plants have been used as potential medication for controlling glucose levels in Diabetes patients. Few studies have explored this effect related to Cissus verticillata L.infusion, though it has been indicated by folk medicine of some Latin American countries.

Interventions

DRUGglibenclamide

5 mg as pills, taken daily during the morning for 60 days

OTHERmedicinal plant infusion

INfusion fo Cissus verticillata L., 1 g in 150 mL water, ingested daily for 60 days.

Sponsors

Conselho Nacional de Desenvolvimento Científico e Tecnológico
CollaboratorOTHER_GOV
Federal University of Paraíba
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* subjects of 30 up to 80 years of age * positive diagnostic for type 2 diabetes mellitus (blood glucose level above 126 mg/dL) * patients that signed the informed consent

Exclusion criteria

* patients with renal and hepatic disfunction, * patients with cardiac problems or other systemic alterations (allergies, pulmonary and gastrointestinal problems) * pregnant women

Design outcomes

Primary

MeasureTime frameDescription
blood glucose60 daysBlood glucose was measured using a Gluco Dr. Plus (AGM-3000) Blood Glucose Monitoring System.

Secondary

MeasureTime frameDescription
Salivary glucose level60 daysThe level of glucose in saliva was measured in laboratory after colleting non-stimulated saliva in test tubes.

Countries

Brazil

Outcome results

None listed

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