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Neurotec in Symptomatic Diabetic Neuropathy

Multi-Centre, Randomised, Double-Blind, Placebo Controlled Trial of the Effect of Neurotec in Symptomatic Diabetic Neuropathy

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT138802201044N3
Enrollment
300
Registered
2009-10-10
Start date
2009-10-10
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Diabetic Neuropathy. Diabetic polyneuropathy

Interventions

Intervention 1: Neurotec 120 mg (1 capsule) two times a day for 4 months and then 120 mg, 1 capsule a day for two month. Intervention 2: Gabapentin 300 mg (1 capsule) two times a day for 4 months and
Treatment - Drugs
Neurotec 120 mg (1 capsule) two times a day for 4 months and then 120 mg, 1 capsule a day for two month
Gabapentin 300 mg (1 capsule) two times a day for 4 months and then 300 mg, 1 capsule a day for 2 months
Placebo 1 identical capsule as active drug two times a day for 4 months and then 1 capsule a day for 2 months

Sponsors

ParsRoos Company
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Pain equivalent to 4 or more on a numerical scale between 0 and 10, Diagnosis of Diabetes Mellitus (Type 1 or 2) defined by American Diabetes Association criteria for at least 3 years, Haemoglobin A1C less than 10%, History of Diabetic Neuropathy for more than a year, Age more than 18 years and less than 60, diagnosis of neuropathy based on Michigan Neuropathy Screening Instrument Exclusion Criteria: Presence of uncontrolled or poor controlled DM, Presence of neuropathy due to other causes than DM, Receiving any investigational drug within 30 days prior to screening, Presence of active or infected diabetic wound, Amputation, Presence of any other systemic or chronic diseases such as: Myopathy, Vasculitis, Peripheral Vascular Diseases, Chronic hepatic or renal diseases, clinically complicating pulmonary, Cardiac, Hematologic, Gastrointestinal, Endocrine disease or Malignancy, Symptomatic degenerative joint disease, active radiculopathy or discopathy, spinal stenosis , active degenerative disc diseases, chronic sciatalgia, sacroiliac joint dysfunction or any chronic painful condition involving lower extremities, apparent or diagnosed psychological problem such as anxiety or depression, Diabetic Retinopathy or retinal haemorrhage, Pregnancy or intention of becoming pregnant during the study period (9 months), Inability to give informed consent according to the agreed process, Corticosteroid therapy, Any drug hypersensitivity, Radiotherapy, Chemotherapy or any immuosuppressive drug use, Electrolyte imbalance

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Baseline, every other week during treatment period (6 months) and every month during follow-up period (3 months). Method of measurement: pain during the last 2 weeks prior to study visits through a Visual Alalogue Scale recorded daily by the patients in diary notebook.;Severity of neuropathy. Timepoint: Baseline, every other week during treatment period (6 months) and every month during follow-up period (3 months). Method of measurement: Neuropathy symptom score.

Secondary

MeasureTime frame
Nurve Conduction Velocity. Timepoint: Baseline, weeks 24 and 36. Method of measurement: Conduction velocity of tibial, proneal and sureal nerves.;Monofilament test. Timepoint: Baseline, weeks 8, 16, 24 and 36. Method of measurement: Monofilament test.;Existence and severity of peripheral neuropathy. Timepoint: Baseline, weeks 8, 16, 24 and 36. Method of measurement: Michigan Neuropathy Score.;Patient's Global Impression of Change (PGIC). Timepoint: Baseline, every other week during treatment period and every month during follow-up period. Method of measurement: 10-point rating scale from very poor condition (1) to very good (10).;Quality of life. Timepoint: Baseline, weeks 16, 24 and 36. Method of measurement: SF-12 questionnaire.;Clinical Global Impression of Change (CGIC). Timepoint: Baseline, every other week during treatment period and every month during follow-up period. Method of measurement: 10-point rating scale from very poor condition (1) to very good (10) determined by the physician.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactPezhman Madani

Endocrine and Metabolism research Center, Tehran University of Medical Sciences

pezhman@iums.ac.ir+98 21 8822 0088

Outcome results

None listed

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