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A STUDY ON SIDDHA HERBAL MEDICINE "AAVARAI KIRUTHAM"FOR THE DIABETES NEUROLOGICAL COMPLICATION(MADHUMEGA AVATHAIGAL)

A RANDOMIZED CONTROLLED TRIAL ON THERAPEUTIC EFFICACY OF SIDDHA HERBAL FORMULATION"AAVARAI KIRUTHAM"IN THE TREATMENT OF MADHUMEGA AVATHAIGAL(VII)-DIABETIC PERIPHERAL NEUROPATHY COMPLICATION OF NON-INSULIN DEPENDENT(TYPE-II)DIABETES MELLITUS - MADHUMEGAM

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/08/020765
Enrollment
60
Registered
2019-08-19
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: E084- Diabetes mellitus due to underlying condition with neurological complications

Interventions

Intervention1: AAVARAI KIRUTHAM: 4ml per oral twice in a day just before meals with milk for 3 months Control Intervention1: not applicable: not applicable

Sponsors

AYOTHIDOSS PANDITHAR HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: BLOOD SUGAR FASTING >126 mg/dl and >200,post prandial blood sugar >200 and 7% AND < 11%,DIABETES PERIPHERAL NEUROPATHY MADHUMEGA AVATHAIGAL,PATIENT WHO IS ALREADY UNDER SIDDHA MEDICATION FOR MADHUMEGAM,DIABETES WITH HYPERTENSION.

Exclusion criteria

Exclusion criteria: AGE BETWEEN 30 YEARS TO 65 YEARS BOTH GENDER,GLYCATED HAEMOGLOBIN 11%, INSULIN DEPENDENT DIABETES MELLITUS,SECONTARY DIABETES MELLITUS,PREGNANT WOMEN AND PLANNING TO BE PREGNANT WITHIN 3 MONTHS,GESTATIONAL DIABETES,EXISTING RENAL FAILURE INDICATED BY ELEVATED SERUM CREATININE LEVELS,CNS DISORDER CORONARY ARTERY DISEASE,THYROID DYSFUNCTION ,MALIGNANT AND ACCELERATED HYPERTENSIVE,SUBJECT THOSE WHO ARE NOT WILLING TO GIVING INFORMED CONCENT.

Design outcomes

Primary

MeasureTime frame
PRIMARY OUTCOME IS ASSESSED BY COMPARING THE BLOOD SUGAR HbA1C LEVEL AND DIABETIC PERIPHERAL NEUROPATHY SCALE BOTH GROUPS BEFORE AND AFTER TREATMENT ASSESMENTTimepoint: 90 DAYS

Secondary

MeasureTime frame
SECONDARY OUTCOME WILL BE ASSESSED BY COMPARING THE FOLLOWING THREE PARAMETERS PRE AND POST TREATMENT CHANGES IN SIDDHA CLINICAL PARAMETERS.EVALUATING CLINICAL LAB PARAMETERS.Timepoint: 90 DAYS

Countries

India

Contacts

Public ContactDR SATHESH KUMAR M K

NATIONAL INSTITUTE OF SIDDHA

drlakshmiramaswamy@gmail.com9025575185

Outcome results

None listed

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