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A Clinical Study of Nerve Pain and Numbness in People with Diabetes, Comparing Habb-e-Azaraqi With Standard Treatment

A Clinical Study on Diabetic Peripheral Neuropathy and Comparative Evaluation of Habb-e-Azaraqi With Standard Control in its Management - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/103937
Enrollment
60
Registered
2026-02-16
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

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

Interventions

Intervention1: Habb-e-Azaraqi: The ingredients of formulation are as follows: Jawitri (Myristica fragrans) 29mg Jaifal (Myristica fragnans) 29mg Darchini (Cinamomoum zeylanicum) 29mg Smagh e Arabi (

Sponsors

Department of Moalajat, Ajmal Khan Tibbiya College, Aligarh Muslim University, Aligarh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Clinically diagnosed patients of diabetic peripheral neuropathy with Type 2 diabetes mellitus through TCNS. Patients between the age of 30 to 60 years of age. Patients of either sex. Controlled case of Type 2 diabetes mellitus either by drug or life style modification. Fasting blood sugar less than or equal to 150 or HbA1c less than or equal to 8. Patients willing to participate in the study and follow the instructions. Washout period of 20 days for patient who were already taking any drug for neuropathy.

Exclusion criteria

Exclusion criteria: Patients below 30 years and above 60 years of age. Uncontrolled case of diabetes mellitus. HbA1c greater than 8. Physiological status: pregnancy and lactation Pathological status: cardiovascular diseases, renal diseases, hepatic diseases, thyroid dysfunction. Complications of diabetes mellitus other than diabetic peripheral neuropathy. Causes of neuropathy other than diabetes. Patient having ischaemic or neuropathic ulcer. Patients taking neurotoxic drugs. Clinically suspected cases of compressive neuropathy. Any comorbid condition. Alcoholics. Severe loss of vibration sensation. VPT value greater than 25 volts. Patients who refuse to give written consent for the study and who fail to follow up.

Design outcomes

Primary

MeasureTime frame
Improvement In Vibration Perception Threshold Value Grade 0 No Loss Of Vibration Perception-Complete Improvement Grade 1 Borderline Loss Of Vibration Perception-Slight Improvement. Grade 2 Mild Loss Of Vibration Perception-Partial Improvement. Grade 3 Moderate Loss Vibration Perception-No Improvement. Improvement In The Score For 10 Gram Monofilament.Timepoint: Assessment Of Vibration Perception Threshold Through Drp At Initiation Of Study (0 Day) And At The End Of Study (60 Days). 10 Miligram Monofilament Test At Initiation Of The Study (0 Day) And At The End Of Study (60 Days).

Secondary

MeasureTime frame
Improvement In The Subjective Parameters: Loss Of Light Touch And Temperature Sensation Numbness And Parasthesia Or Both In Feet And Hands Pain Symptoms Icluding Burning Allodynia (Contact Pain).Timepoint: Assessment On 0, 15, 30, 45 And 60 Days.

Countries

India

Contacts

Public ContactTabi Idris Siddiqui

Ajmal Khan Tibbiya College, Faculty of Unani Medicine, Aligarh Muslim University, Aligarh

mursaleennaseer1@gmail.com9412562724

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026