Skip to content

Gymnema Caplets in Pre Diabetis

Efficacy and Safety of Gymnema Caplets in Pre Diabetic Subjects; A Double Blind Placebo Controlled Clinical Study.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/05/013956
Enrollment
60
Registered
2018-05-17
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Subjects with Prediabetic conditions.

Interventions

Intervention1: Gymnema Caplets: 1 caplet twice daily for a period of 12 weeks. Control Intervention1: Placebo: 1 caplet twice daily for a period of 12 weeks.

Sponsors

The Himalaya Drug Company
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Subjects of both sexes aged 18 and above. 2 Subjects with fasting blood sugar levels of 100mg/dl to 125mg/dl and/or HbA1c value of 5.7% to 6.4%. 3 Subjects with one or more of the following known risk factors-Hypertension, hypercholesterolemia, obesity, and familial history of diabetes, gestational diabetes, and known impaired glucose tolerance. 4 Subjects willing to sign informed consent form.

Exclusion criteria

Exclusion criteria: 1 Women who are pregnant, planning to conceive, or nursing an infant. 2 Not willing to sign informed consent form.

Design outcomes

Primary

MeasureTime frame
1 Fasting blood sugar levels. 2 Post prandial blood sugar levels. 3 Glycolated Haemoglobin.Timepoint: At Screening, At Week 4, At Week 8 and At Week 12

Secondary

MeasureTime frame
Haematology and Biochemical investigationsTimepoint: At Screening, At Week 4, At Week 8 and At Week 12

Countries

India

Contacts

Public ContactDr Padmanabha

Institute of Ayurveda and Integrative medicine (I-AIM)

shree_subrahmanya@frlht.org080-285657000

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026