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Homoeopathic treatment of nnumbness, tingling, aching, and burning pain, hyperesthesia, and weakness of limbs in adults with high blood sugar.

Efficacy of individualized homeopathic medicines in the treatment of peripheral diabetic neuropathy in adults A double-blind, randomized, placebo-controlled trial with mutual antidiabetic standard care - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/093559
Enrollment
142
Registered
2025-08-25
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: E11- Type 2 diabetes mellitus

Interventions

Intervention1: Individualized homoeopathic medicines plus Standard care and Concomitant care: Intervention is planned as administering indicated homoeopathic medicines in centesimal potencies (CH). Ea

Sponsors

D N De Homoeopathic Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Adults aged of 30-65 years 2. Participant of either sex or transgender. 3. person who had been diagnosed with diabetic neuropathy for at least 3 months. 4. DNE score greater than 3.

Exclusion criteria

Exclusion criteria: 1. Individuals with other neurological disorders. 2. Abnormal gait, loss of arch with multiple fractures in tarsal bones wrist, foot drop. 3. Diabetic complications (such as retinopathy or renal involvement with history of recurrent acute complaints like hypoglycaemia, keto-acidosis). 4. Self-reported immune-compromised state. 5. Tobacco chewing and/or smoking, alcoholism and/or any other form(s) of substance abuse and/or dependence. 6. Pregnant or lactating women, unstable mental health. 7. Those who requiring insulin with an HbA1c equal or more than 10. 8. Participants who had received homeopathic treatment for chronic diseases in the last 6 months or were critically ill were also excluded from the study. 9. patient not providing with written informed consent voluntarily. 10. Vulnerable population-Unconscious, non-ambulatory, too sick for consultation, differently abled, terminally ill or critically ill patients, mentally incompetent people.

Design outcomes

Primary

MeasureTime frame
Neuropathy total symptom score(NTSS-6)Timepoint: Baseline, every months up to three months

Secondary

MeasureTime frame
Douleur Neuropathique 4 Questions (DN4) scaleTimepoint: Baseline, every months up to three months;Diabetic Neuropathy Examination (DNE) scoreTimepoint: Baseline, every months up to three months;Measure Yourself Medical outcome Profile version 2 (MYMOP-2) scoreTimepoint: Baseline, every months up to three months;Fasting blood sugar (FBS), Postprandial blood sugar (PPBS)Timepoint: Baseline, every months up to three months;HbA1C%, lipid profile, liver enzymes (ALT, AST), urea, creatinine, urine profileTimepoint: At baseline and after three months of interventions

Countries

India

Contacts

Public ContactSUBHRANIL SAHA

D N DE HOMOEOPATHIC MEDICAL COLLEGE AND HOSPITAL

asamiul504@gmail.com6290039839

Outcome results

None listed

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