Skip to content

"To study the combined effect of Emblica officinalis (amla) and Curcuma longa (Haldi)on blood sugar level in type 2 Diabetes Mellitus".

"Clinical evaluation of Nishamalaki in type 2 Diabetes Mellitus".

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2014/06/004686
Enrollment
40
Registered
2014-06-19
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- patients suffering from type 2 diabets mellietus, on oral hypoglycemic agents.

Interventions

Intervention1: Nishamalaki: Nishamalaki is a drug made from emblica officinalis and curcuma longa route of administration -- Oral Dosage 4gms once daily, early in the morning on empty stomach
with 0.2ml of honey Control Intervention1: Tab Metformin Tab Glimepiride: Tab Metformin less than 1000 mg/day and/or Tab Glimepiride less than 3mg/day. Oral hypo gylcemic agents Dose used by the s
Frequency of administration- as per the blood sugar level. the dosage will be modified as per the patients responds to the treatment

Sponsors

Dr Mrs VAPandit
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients satisfying all the following criteria would be included in the study: 1. Ready to abide by trial procedures and to give informed consent. 2. Either sex above 40 yrs 3. Type 2 diabetes mellitus for 4. Fasting blood glucose between 126- 234 mg % and post-prandial blood glucose (after a standard meal) between 162mg% to 360mg% 5. HbA1c between 7.0-9.5 %.

Exclusion criteria

Exclusion criteria: Patients suffering from any of the following conditions will be excluded from the study: a. Type 1 diabetes mellitus b. Patients with psychiatric disorder. c. Patients with H/o hematological disorders d. Complications of diabetes

Design outcomes

Primary

MeasureTime frame
To determine the effect of addition of Nishamalaki in patients of type II DM on oral hypoglycemic (OHA) agents on 1) Blood sugar level 2) HbA1c Timepoint: 0-3months

Secondary

MeasureTime frame
To determine the effect of addition of Nishamalaki in patients of type II DM on oral hypoglycemic (OHA) agents on 1) Adverse reactions 2) Changes in the doses of OHAs Timepoint: 0-3months

Countries

India

Contacts

Public ContactDr Jayshree Dawane

Bharati vidyapeeth deemed medical university

swapnil5_us@yahoo.com9773326619

Outcome results

None listed

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