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A study of Pregabalin IP 75 mg and Nortriptyline 10 mg Tablets in patients with diabetic peripheral neuropathy

Phase 4
Completed
Conditions
Health Condition 1: G64- Other disorders of peripheral nervous system
Registration Number
CTRI/2022/02/040438
Lead Sponsor
Micro Labs Limited
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
203
Inclusion Criteria

1. Presence of type 2 diabetes mellitus

2. No change in anti-diabetic medication for the past 1 month

3. Evidence of painful diabetic neuropathy by:

i.Neuropathic pain present for at least 1 month.

ii.Mean pain intensity of more than 50% by patient assessment by NRS (numerical rating scale)

4. Ability to understand and the willingness to sign and date a written informed consent document at the screening visit before any protocol specific procedures are performed

Exclusion Criteria

1. Pregnancy and lactation.

2. Subjects having intolerance, hypersensitivity or any other contraindication to any of the Investigational products.

3. Evidence of other causes for neuropathy and painful conditions

4. Epilepsy, psychiatric and cardiac diseases, hypertensives not on treatment, peripheral vascular disease and substance abuse.

5. Intake of any other anticonvulsants, antidepressants, membrane stabilizers and opioid

6. Patients who have participated in another clinical study in the past 3 months prior to commencement of this study

7. Subjects judged unfit for this study by investigator.

Study & Design

Study Type
PMS
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Decrease in mean pain scoreTimepoint: week 0, week 2, week 4
Secondary Outcome Measures
NameTimeMethod
Improvement in daily pain related symptoms scale SIRS scaleTimepoint: week 0, week 2, week 4;Improvement in Patients Global Impression of Change (PGIC)Timepoint: week 0, week 2, week 4
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