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A study to compare Pramehari Churna and a Polyherbal medicine in people with Prediabetes

Effectiveness of Pramehari Churna in comparison with Polyherbal combination in management of Prediabetes : A randomized Controlled Trial - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/105846
Enrollment
64
Registered
2026-03-10
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: R739- Hyperglycemia, unspecified

Interventions

None listed

Sponsors

Dr Arshid Shekh Jabir Shekh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Patients having hyperglycemia confirmed by La- boratory Investigation, i.e., OGTT 140 to 199 mg/dl and HbA1c 5.7% to 6.4% 2) Age group between 25 years and 60 years, newly diagnosed with prediabetes within 3 months. 3) Patient willing to sign the consent form for the clinical trial.

Exclusion criteria

Exclusion criteria: 1) Those reporting prior use of medication to treat diabetes mellitus. 2) Alcoholic liver disease, cirrhosis, liver cancer, autoimmune disease; had symptoms of kidney failure or on renal dialysis, 3) Taking steroids for any illness. 4) Gestational diabetes 5) Pregnancy or breastfeeding 6) Previously participate in any study of investigational drugs within 1 month before this study

Design outcomes

Primary

MeasureTime frame
This study may provide the better drug of choice for reducing the signs and symptoms of prediabetes that will be assessed after treatment with Pramehari churna and Polyherbal combination.Timepoint: At the end of 30 days (1, 15, 30 days)

Secondary

MeasureTime frame
It may have decreased the severity of observed signs and symptoms.Timepoint: At the end of 30 days (1, 15, 30 days interval)

Countries

India

Contacts

Public ContactDr Arshid Shekh Jabir Shekh

Shri Ayurved Mahavidyalaya, Nagpur

dr.dachewar@gmail.com9822206312

Outcome results

None listed

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