Efficacy of Pregabalin for Diabetic Pruritus - A Randomized Controlled Study.
Condition(s) studied
Investigational drug(s) / intervention(s)
Pregabalin 75 mg: 75 mg of pregabalin will be given at night for the intervention group along with emollient local application
Placebo Oral Capsule: placebo capsule will be identical in appearance to the pregabalin capsule. it will be given at the same time of the day like pregabalin. same Emollient which is used in the Intervention arm will be applied locally on the areas of itching, morning after bathing .
Study summary
Brief Summary:
The goal of this randomized controlled study is to learn if pregabalin combined with emollients can reduce pruritus (itching) in people with Type 2 Diabetes Mellitus. The main questions it aims to answer are:
Does pregabalin combined with emollients reduce pruritus severity compared to a placebo combined with emollients? What is the impact of pregabalin on the quality of life of participants suffering from diabetic pruritus? we will compare pregabalin plus emollient to a placebo plus emollient to see if pregabalin works better for reducing pruritus.
Participants will:
Receive either pregabalin 75 mg daily along with emollient therapy or a placebo along with emollient therapy.
Visit the clinic at weeks 4, 8, and 12 for follow-up assessments, including:
Pruritus severity using the Visual Analog Scale (VAS) and 5-D Itch Scale. Patient Global Impression of Change (PGIC) to measure overall improvement. This study will help determine if pregabalin, a drug used for neuropathic pain, can be an effective treatment for pruritus in people with diabetes.
Eligibility
Primary outcome measure(s)
- • Mean change in VAS (Visual analogue scale)scores from baseline to week 12 between the two groups. — 12 weeks
For all patients baseline VAS score will be assessed , then for both the intervention groups , follow up VAS scores will be noted at week 4, 8 and 12 weeks. Mean change in VAS scores in both the groups before and after the intervention will be the Primary outcome.
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Department of Endocrinology , PGIMER, Chandigarh | Chandigarh | Chandigarh | Not Yet Recruiting |
| Department of Endocrinology , PGIMER, Chandigarh | Chandigarh | Chandigarh | Recruiting |
More Post Graduate Institute of Medical Education and Research, Chandigarh trials in India
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06790537 on ClinicalTrials.gov ↗ ← All trials in India