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Assessing the effect of Efficacy of Habb-e-Asgandh in Diabetic Peripheral Neuropathy

Evaluating the Therapeutic Efficacy of Habb-e-Asgandh in Diabetic Peripheral Neuropathy, A Randomized Single Blind Standard Control Study.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/03/041293
Enrollment
40
Registered
2022-03-23
Start date
Unknown
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

Health Condition 1: - Health Condition 2: E114- Type 2 diabetes mellitus with neurological complications

Interventions

Intervention1: Habb- e- Asgandh: dosage of intervention drug is 2 pills (each 650mg) at bed time for 45 days. Control Intervention1: Tab. pregabalin: 75mg of tab. pregabalin is to be given once a day

Sponsors

Central Council of Research in Unani Medicine New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Clinically diagnosed patients of Diabetic Peripheral Neuropathy with type 2 Diabetes mellitus, having fasting blood sugar (FBS) from 140mg/dl up to 200mg/dl and post prandial (PPS) level from 200mg/dl up to 300mg/dl. - Patients between the ages of 30 to 60 years. 1. Patients irrespective of gender. 2. Patients having blood urea, serum creatinine, SGOT, SGPT within normal limit. 3. Patients willing to participate in the study and follow the instructions.

Exclusion criteria

Exclusion criteria: 1. Pregnant and lactating mothers 2. Pathological status: cardiovascular disease, renal disease, hepatic disease. 3. Patients below 30 years and above 60 years of age. ï?? Complications of Diabetes other than Diabetic peripheral neuropathy. 4. Causes of Neuropathy other than Diabetes. 5. Patients who refuse to give the written consent for the study

Design outcomes

Primary

MeasureTime frame
Diabetic Peripheral Neuropathy will be assessed by Toronto Clinical Neuropathy ScoreTimepoint: on 0 day, 15th day, 30th day and 45th day.

Secondary

MeasureTime frame
Haematological tests include Hb%, TLC, DLC, ESR and Biochemical tests include Fasting blood sugar, Post prandial blood sugar, blood urea, serum creatinine, serum bilurubin, SGOT, SGPT, Total protein, Alkaline phosphataseTimepoint: before (0th day) and after intervention (45th day)

Countries

India

Contacts

Public ContactDr Zaffar Hussain

Regional Research Institute of Unani Medicine, Srinagar

hussainzaffar6@gmail.com7006021996

Outcome results

None listed

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