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Effect of Polyherbal Compound for Control of Blood Sugar in Impaired Glucose Tolerance and Diabetes

A Polyherbal for Control of Blood Sugar in Subjects With Impaired Glucose Tolerance and/or Early Type 2 Diabetes. A Randomized Placebo Controlled Study of a Polyherbal (Whole Herb Formulation)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02866539
Enrollment
122
Registered
2016-08-15
Start date
2016-12-31
Completion date
2018-01-15
Last updated
2018-04-11

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

Conditions

Diabetes Mellitus

Brief summary

The aim of the study is to control blood sugar with Sugar Balance capsules which is the leaves of three herbs: ivy ground (Coccinia indica)-200mg, bougainvillia (Bougainvillea spectabilis)-30mg, Madagascar periwinkle (Catharanthus rosea)-20mg.

Interventions

A unique combination of 3 herbs that lower blood sugars

DRUGPlacebo

Similar looking inactive powder

Sponsors

Composite Interceptive Med Science
Lead SponsorINDUSTRY

Study design

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

Eligibility

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

Inclusion criteria

* Adult males and non-pregnant females aged ≥30 years having a diagnosis of pre-diabetes (impaired fasting glucose or impaired glucose tolerance) and a diabetes and a meeting one of the following criteria 1. Fasting Plasma Glucose ≥100 mg/dL, fasting is defined as no caloric intake for at least 8 h, OR 2. 2-h Post load Glucose ≥140 mg/dL during an Oral Glucose Tolerance Test (OGTT). The test should be performed as described by the World Health Organisation(WHO), using a glucose load containing the equivalent of 75 g anhydrous glucose dissolved in water. OR 3. Glycosylated haemoglobin (A1C) ≥5.7%. The test should be performed in a laboratory using a method that is National Accreditation Board for Testing and Calibration Laboratories certified and standardized. OR 4. In a patient with classic symptoms of hyperglycaemia or hyperglycaemic crisis, a random plasma glucose ≥200 mg/dL in the last 12 months.

Exclusion criteria

* Any one of the following 1. History of diabetes onset \>12 months from date of randomization and/or on any oral hypoglycemic agents (other than metformin) 2. Any history suggestive of micro vascular or macro vascular disease 3. Women in childbearing age unable to practice any form of contraception 4. Impaired renal function; estimated glomerular filtration rate(eGFR) \<60mls/min/1.73m2. 5. Known history of any chronic illness taking regular pharmacological agents. 6. Blood pressure fluctuations exceeding 10 mmHg on 2 subsequent clinic visits or known history of hypotension or bradycardia in last 6 months or taking 2 or more antihypertensive medications regularly in the last 6 weeks 7. Current or former employees of organic India 8. Participating in another clinical trial with an active intervention or drug or device with last dose taken within 60 days. 9. Refusing consent or physician uncomfortable with patient compliance to treatments or follow up.

Design outcomes

Primary

MeasureTime frameDescription
Number of diabetes subjects achieving glycemic control6 monthsa 0.5% reduction in baseline A1c and/or fasting plasma glucose below 125 mg/dl or 2 hour postprandial glucose \<180 mg/dl
Number of pre-diabetes achieving euglycemic status6 monthsmeasured as A1c \< 5.7% and/or fasting plasma glucose \<100mg/dl/

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026