Diabetic PruritusPhase 4PREDICTNCT06790537
Efficacy of Pregabalin for Diabetic Pruritus - A Randomized Controlled Study.
A Phase 4 study testing Pregabalin 75 mg in people with Diabetic Pruritus and Efficacy of Pregabalin in Controlling Diabetic Pruritus Severity, run by Post Graduate Institute of Medical Education and Research, Chandigarh at 2 sites in India.
Trial 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. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Diabetic Pruritus, Efficacy of Pregabalin in Controlling Diabetic Pruritus Severity
- What is being tested?
- Pregabalin 75 mg
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 46 participants
- Where
- 2 sitesIndia
- Study dates
- 17 Apr 2025to 30 Jun 2026
- Phase
- Phase 4
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Adults (>18 years) with Type 2 Diabetes Mellitus
- HbA1c <10% and on stable medication for at least 1 month before enrolment.
- Presence of chronic pruritus (lasting for six weeks or longer) [2].
- Generalized or localised pruritus affecting more than one major body area*
- Baseline VAS score of ≥5 $ *Pruritus including Generalized or localized pruritus as long as it involves two or more areas as per the 5D Itch Scale distribution [Head/scalp, face, chest, abdomen, back, buttocks, thighs, lower legs, feet/toes, arms, palms, hands/fingers, groin, and clothing contact points (waistbands/undergarments).
- $ Baseline VAS score of ≥5 is included to ensure sufficient severity of pruritus for measurable improvement.
Who cannot join
- Types of Diabetes:
- o Gestational Diabetes, pregnant and breastfeeding women with T2DM, Type 1 DM.
- Pruritus Duration and Causes:
- Pruritus of less than six weeks' duration.
- Pruritus associated with systemic conditions such as uraemia (CKD stage IV/V), cholestatic liver diseases, viral hepatitis, HIV infection, uncontrolled hypothyroidism* or hyperthyroidism^, myeloproliferative disorders, Chronic venous insufficiency in legs or Postherpetic pruritus.
- Uncontrolled hypothyroidism - T3 / T4 below the upper limit of normal.
Show all 17Show fewer
- ^Uncontrolled hyperthyroidism- T3/T4 above the upper limit of normal.
- Pruritus due to primary dermatological disorders presenting with skin lesions (e.g., atopic dermatitis, eczema, psoriasis, allergic contact dermatitis, urticarial disorders, lichen planus, prurigo nodularis, asteatotic dermatitis).
- Use of Medications Affecting Pruritus:
- o Current or recent use (within 2 weeks before study initiation) of systemic treatments that may impact pruritus, including gabapentins (e.g., pregabalin, gabapentin), tricyclic antidepressants (TCA), antihistamines, corticosteroids, and calcineurin inhibitors.
- Rationale: Since these medications are commonly used for neuropathic pain or Pruritus which coexists with diabetic pruritus, their recent use may affect pruritus severity and treatment response. Patients using these drugs for neuropathic pain or other conditions should undergo a washout period of 2 weeks before study initiation.
- Drug Hypersensitivity and Reactions:
- o Known allergies or hypersensitivity to pregabalin or emollient.
- Psychiatric and Immunocompromised Status:
- Severe psychiatric disorders that may interfere with the evaluation of pruritus or adherence to the study protocol.
- Immunocompromised patients (e.g., post-transplant, immunosuppressive therapy). Pruritus due to Notalgia paresthetica or brachioradial pruritus, post burn pruritus, opioid-induced pruritus.
- People with Substance abuse disorders.
Trial locations and contacts
2 sites in 1 country. Contact the study team or a site near you to ask about taking part.
India2 sites, 2 recruiting
- Not yet recruiting
Department of Endocrinology , PGIMER, Chandigarh
Chandigarh, Chandigarh, 160012
Karthik N Dr, Senior Resident,endocrinolgy, +919492115369, nalam.karthik8788@gmail.com
Ashu Rastogi Dr, DM ENDOCRINOLOGY, ashuendo@gmail.com
- Recruiting
Department of Endocrinology , PGIMER, Chandigarh
Chandigarh, Chandigarh, 160012
Karthik N Dr, Senior Resident,endocrinolgy, +919767790622, nalam.karthik8788@gmail.com
Ashu Rastogi Dr, DM ENDOCRINOLOGY, +9197810101046 ext. +919781001046, ashuendo@gmail.com
About this study
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:
Read more
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.
Read the detailed description
Introduction Pruritus, commonly referred to as itching, is a common symptom experienced by patients with diabetes mellitus (DM). It is associated with both physical discomfort and significant psychological distress, affecting the overall quality of life (QoL). While acute pruritus may act as a protective response to harmful stimuli, chronic pruritus lasting for more than six weeks often signals an underlying pathology. In diabetic patients, pruritus can result from a combination of metabolic, neuropathic, and dermatological factors, leading to persistent symptoms. Despite its high prevalence, effective treatments for diabetic pruritus remain limited.
Pruritus in diabetes mellitus is complex, often resulting from diabetic neuropathy, skin barrier dysfunction (xerosis), and oxidative stress. Although treatments like emollients and antihistamines are used, their effectiveness is often suboptimal, particularly since diabetic pruritus is primarily non-histaminergic in nature. Pregabalin, a medication commonly used for neuropathic pain, has shown promise in treating neuropathic pruritus. Given the neuropathic component of diabetic pruritus, pregabalin may provide an effective treatment option when combined with emollients to address skin dryness.
Rationale for the Study Diabetic pruritus presents a significant challenge due to its multifactorial nature. While various treatments such as topical agents and antihistamines are used, they do not effectively address the underlying neuropathic component of pruritus in diabetic patients. Pregabalin, by modulating calcium channels and reducing neuronal excitability, has demonstrated efficacy in treating neuropathic pruritus in conditions such as uremic pruritus. Considering that diabetic pruritus shares similar neuropathic mechanisms, pregabalin could represent a valuable treatment option for reducing pruritus severity.
Additionally, xerosis (dry skin) is a common issue in diabetic patients and contributes significantly to pruritus. Emollient therapy helps restore moisture to the skin, addressing this underlying factor. The combination of pregabalin and emollient therapy may therefore provide a synergistic effect, reducing pruritus severity and improving the QoL of diabetic patients.
Aim:
To assess the efficacy of pregabalin combined with emollient therapy in reducing the severity of pruritus in patients with Type 2 Diabetes Mellitus (T2DM), compared to a placebo combined with emollient therapy.
Primary and Secondary objectives:
Primary Objective:
VAS Score: The mean change in VAS scores from baseline to week 12 between the pregabalin and placebo groups. The VAS measures pruritus severity, where patients rate their itch intensity from 0 (no itch) to 10 (worst imaginable itch).
Secondary Objective :
Proportion of participants achieving a minimum 3-point reduction in VAS scores at week 12.
Mean change in VAS scores at weeks 4 and 8. 5-D Itch Scale: A multidimensional scale measuring pruritus across five domains: duration, degree, direction, disability, and distribution.
PGIC Scores: The Patient Global Impression of Change scale is a subjective measure of the patient's overall perception of improvement, assessed at weeks 4, 8, and 12.
Safety Profile: Incidence and severity of adverse events (AEs) during the study period.
Discontinuation Rates: Rates of participant withdrawal due to adverse events in both treatment groups.
Inclusion Criteria:
Adults aged >18 years with Type 2 Diabetes Mellitus. HbA1c <10% with stable medication for at least 1 month before enrollment. Chronic pruritus lasting for six weeks or longer. Generalized or localized pruritus affecting more than one major body area as per the 5-D Itch Scale distribution.
Baseline VAS score ≥ 5.
Exclusion Criteria:
Type 1 Diabetes Mellitus, gestational diabetes, pregnant or breastfeeding women.
Pruritus duration of less than six weeks. Pruritus associated with conditions such as uremia (CKD stage IV/V), cholestasis, viral hepatitis, HIV, uncontrolled hypothyroidism, uncontrolled hyperthyroidism, and others.
Pruritus due to primary dermatological disorders (e.g., eczema, psoriasis, lichen planus).
Recent use of systemic treatments affecting pruritus, including gabapentins, tricyclic antidepressants, antihistamines, corticosteroids, or calcineurin inhibitors (within 2 weeks before study initiation).
Known hypersensitivity to pregabalin or emollients. Severe psychiatric disorders that may interfere with the evaluation of pruritus or adherence to the study.
Immunocompromised patients (e.g., post-transplant, immunosuppressive therapy). Methodology
Study Design:
This is a double-blind, randomized controlled trial (RCT). Both participants and researchers will be unaware of the treatment allocation, ensuring unbiased results.
Study Population:
The study will include adults aged 18 and above, diagnosed with Type 2 Diabetes Mellitus, who are experiencing chronic pruritus for at least six weeks.
Intervention:
Group A (Intervention): Pregabalin 75 mg daily at night + emollient therapy. Group B (Control): Placebo (identical to pregabalin) + emollient therapy.
Randomization:
Participants will be randomly assigned to one of the two treatment groups using a computer-generated randomization schedule to maintain allocation concealment.
Follow-up and Assessments:
Participants will attend follow-up visits at weeks 4, 8, and 12 for:
Pruritus severity assessment using VAS and 5-D Itch Scale. PGIC evaluation to assess subjective improvement. Safety monitoring for adverse events.
Statistical Analysis:
The primary endpoint is the change in VAS scores from baseline to week 12. Secondary endpoints include changes in the 5-D Itch Scale, PGIC scores, and safety assessments.
Appropriate statistical tests (e.g., t-tests, chi-square tests) will be used for comparisons between groups.
Ethical Considerations This study will be conducted in accordance with ethical guidelines provided by the Declaration of Helsinki and Good Clinical Practice (GCP). Ethical approval will be obtained from the Institutional Ethics Committee (IEC) of PGIMER, Chandigarh, and informed consent will be obtained from all participants.
Conclusion This study aims to evaluate the efficacy of pregabalin in treating diabetic pruritus, a common and troublesome symptom for diabetic patients. The combination of pregabalin and emollients may provide a novel, effective approach for managing pruritus and improving the quality of life for those affected.
- Being tested
- Pregabalin 75 mg, Placebo Oral Capsule
- Keywords
- Efficacy of pregabalin for control of generalised pruritus in Diabetic patients
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Pregabalin 75 mgDrug
75 mg of pregabalin will be given at night for the intervention group along with emollient local application
Placebo Oral CapsuleOther
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 group | Role | What they receive |
|---|---|---|
| Intervention group | Experimental | Pregabalin with emollient group. Pregabalin 75 mg one dose at night plus emollient application in the morning after bathing. Receives: Drug: Pregabalin 75 mg |
| placebo arm | Placebo comparator | Placebo pill identical in appearance to the pregabalin capsule and standard treatment with emollient application locally on the areas of itching . Receives: Other: Placebo Oral Capsule |
What is being measured
The primary outcome is the main question the study is designed to answer.
• Mean change in VAS (Visual analogue scale)scores from baseline to week 12 between the two groups.
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.
Measured: 12 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Jan 2025
- Study start17 Apr 2025
- Primary completion30 Jun 2026 (estimated)
- Study completion30 Jun 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Diabetic PruritusStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 4
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind
- Who is masked
- Participant, Investigator, Outcomes assessor
- Enrolment
- 46 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Post Graduate Institute of Medical Education and Research, Chandigarh
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Ashu Rastogi, Post Graduate Institute of Medical Education and Research, Chandigarh
- Investigators
- Ashu Rastogi, DM ENDOCRINOLOGY, Principal investigator, Post Graduate Institute of Medical Education and Research, Chandigarh
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06790537
- Sponsor's protocol ID
- PREDICT
- Acronym
- PREDICT
- Status last verified
- Jan 2025
- First submitted
- 18 Jan 2025
- Last updated
- 5 Jan 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 5 Jan 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Efficacy of Pregabalin for Diabetic Pruritus - A Randomized Controlled Study.
- ClinicalTrials.gov ID
- NCT06790537
- Acronym / sponsor ID
- PREDICT / PREDICT
- Keywords
- Efficacy of pregabalin for control of generalised pruritus in Diabetic patients
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 46 participants (estimated)
- Lead sponsor
- Post Graduate Institute of Medical Education and Research, ChandigarhUniversity, hospital or other
- Study start
- 17 Apr 2025 (actual)
- Primary completion
- 30 Jun 2026 (estimated)
- Study completion
- 30 Jun 2026 (estimated)
- First posted
- 24 Jan 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
Introduction Pruritus, commonly referred to as itching, is a common symptom experienced by patients with diabetes mellitus (DM). It is associated with both physical discomfort and significant psychological distress, affecting the overall quality of life (QoL). While acute pruritus may act as a protective response to harmful stimuli, chronic pruritus lasting for more than six weeks often signals an underlying pathology. In diabetic patients, pruritus can result from a combination of metabolic, neuropathic, and dermatological factors, leading to persistent symptoms. Despite its high prevalence, effective treatments for diabetic pruritus remain limited.
Pruritus in diabetes mellitus is complex, often resulting from diabetic neuropathy, skin barrier dysfunction (xerosis), and oxidative stress. Although treatments like emollients and antihistamines are used, their effectiveness is often suboptimal, particularly since diabetic pruritus is primarily non-histaminergic in nature. Pregabalin, a medication commonly used for neuropathic pain, has shown promise in treating neuropathic pruritus. Given the neuropathic component of diabetic pruritus, pregabalin may provide an effective treatment option when combined with emollients to address skin dryness.
Rationale for the Study Diabetic pruritus presents a significant challenge due to its multifactorial nature. While various treatments such as topical agents and antihistamines are used, they do not effectively address the underlying neuropathic component of pruritus in diabetic patients. Pregabalin, by modulating calcium channels and reducing neuronal excitability, has demonstrated efficacy in treating neuropathic pruritus in conditions such as uremic pruritus. Considering that diabetic pruritus shares similar neuropathic mechanisms, pregabalin could represent a valuable treatment option for reducing pruritus severity.
Additionally, xerosis (dry skin) is a common issue in diabetic patients and contributes significantly to pruritus. Emollient therapy helps restore moisture to the skin, addressing this underlying factor. The combination of pregabalin and emollient therapy may therefore provide a synergistic effect, reducing pruritus severity and improving the QoL of diabetic patients.
Aim:
To assess the efficacy of pregabalin combined with emollient therapy in reducing the severity of pruritus in patients with Type 2 Diabetes Mellitus (T2DM), compared to a placebo combined with emollient therapy.
Primary and Secondary objectives:
Primary Objective:
VAS Score: The mean change in VAS scores from baseline to week 12 between the pregabalin and placebo groups. The VAS measures pruritus severity, where patients rate their itch intensity from 0 (no itch) to 10 (worst imaginable itch).
Secondary Objective :
Proportion of participants achieving a minimum 3-point reduction in VAS scores at week 12.
Mean change in VAS scores at weeks 4 and 8. 5-D Itch Scale: A multidimensional scale measuring pruritus across five domains: duration, degree, direction, disability, and distribution.
PGIC Scores: The Patient Global Impression of Change scale is a subjective measure of the patient's overall perception of improvement, assessed at weeks 4, 8, and 12.
Safety Profile: Incidence and severity of adverse events (AEs) during the study period.
Discontinuation Rates: Rates of participant withdrawal due to adverse events in both treatment groups.
Inclusion Criteria:
Adults aged >18 years with Type 2 Diabetes Mellitus. HbA1c <10% with stable medication for at least 1 month before enrollment. Chronic pruritus lasting for six weeks or longer. Generalized or localized pruritus affecting more than one major body area as per the 5-D Itch Scale distribution.
Baseline VAS score ≥ 5.
Exclusion Criteria:
Type 1 Diabetes Mellitus, gestational diabetes, pregnant or breastfeeding women.
Pruritus duration of less than six weeks. Pruritus associated with conditions such as uremia (CKD stage IV/V), cholestasis, viral hepatitis, HIV, uncontrolled hypothyroidism, uncontrolled hyperthyroidism, and others.
Pruritus due to primary dermatological disorders (e.g., eczema, psoriasis, lichen planus).
Recent use of systemic treatments affecting pruritus, including gabapentins, tricyclic antidepressants, antihistamines, corticosteroids, or calcineurin inhibitors (within 2 weeks before study initiation).
Known hypersensitivity to pregabalin or emollients. Severe psychiatric disorders that may interfere with the evaluation of pruritus or adherence to the study.
Immunocompromised patients (e.g., post-transplant, immunosuppressive therapy). Methodology
Study Design:
This is a double-blind, randomized controlled trial (RCT). Both participants and researchers will be unaware of the treatment allocation, ensuring unbiased results.
Study Population:
The study will include adults aged 18 and above, diagnosed with Type 2 Diabetes Mellitus, who are experiencing chronic pruritus for at least six weeks.
Intervention:
Group A (Intervention): Pregabalin 75 mg daily at night + emollient therapy. Group B (Control): Placebo (identical to pregabalin) + emollient therapy.
Randomization:
Participants will be randomly assigned to one of the two treatment groups using a computer-generated randomization schedule to maintain allocation concealment.
Follow-up and Assessments:
Participants will attend follow-up visits at weeks 4, 8, and 12 for:
Pruritus severity assessment using VAS and 5-D Itch Scale. PGIC evaluation to assess subjective improvement. Safety monitoring for adverse events.
Statistical Analysis:
The primary endpoint is the change in VAS scores from baseline to week 12. Secondary endpoints include changes in the 5-D Itch Scale, PGIC scores, and safety assessments.
Appropriate statistical tests (e.g., t-tests, chi-square tests) will be used for comparisons between groups.
Ethical Considerations This study will be conducted in accordance with ethical guidelines provided by the Declaration of Helsinki and Good Clinical Practice (GCP). Ethical approval will be obtained from the Institutional Ethics Committee (IEC) of PGIMER, Chandigarh, and informed consent will be obtained from all participants.
Conclusion This study aims to evaluate the efficacy of pregabalin in treating diabetic pruritus, a common and troublesome symptom for diabetic patients. The combination of pregabalin and emollients may provide a novel, effective approach for managing pruritus and improving the quality of life for those affected.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Intervention group | Experimental | Drug: Pregabalin 75 mgPregabalin with emollient group. Pregabalin 75 mg one dose at night plus emollient application in the morning after bathing. |
| placebo arm | Placebo comparator | Other: Placebo Oral CapsulePlacebo pill identical in appearance to the pregabalin capsule and standard treatment with emollient application locally on the areas of itching . |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- Adults (>18 years) with Type 2 Diabetes Mellitus
- HbA1c <10% and on stable medication for at least 1 month before enrolment.
- Presence of chronic pruritus (lasting for six weeks or longer) [2].
- Generalized or localised pruritus affecting more than one major body area*
- Baseline VAS score of ≥5 $ *Pruritus including Generalized or localized pruritus as long as it involves two or more areas as per the 5D Itch Scale distribution [Head/scalp, face, chest, abdomen, back, buttocks, thighs, lower legs, feet/toes, arms, palms, hands/fingers, groin, and clothing contact points (waistbands/undergarments).
Key exclusion criteria (17 listed)
- Types of Diabetes:
- o Gestational Diabetes, pregnant and breastfeeding women with T2DM, Type 1 DM.
- Pruritus Duration and Causes:
- Uncontrolled hypothyroidism - T3 / T4 below the upper limit of normal.
- ^Uncontrolled hyperthyroidism- T3/T4 above the upper limit of normal.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Pregabalin 75 mg75 mg of pregabalin will be given at night for the intervention group along with emollient local application | Drug | Intervention group |
| Placebo Oral Capsuleplacebo 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 . | Other | placebo arm |
Primary outcome
• Mean change in VAS (Visual analogue scale)scores from baseline to week 12 between the two groups.
Time frame: 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.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 Jan 2026.
- Individual participant dataSharing planned: Undecided
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Ashu Rastogi, DM ENDOCRINOLOGY principal investigator
Post Graduate Institute of Medical Education and Research, Chandigarh
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing Pregabalin 75 mg in people with Diabetic Pruritus and Efficacy of Pregabalin in Controlling Diabetic Pruritus Severity, run by Post Graduate Institute of Medical Education and Research, Chandigarh at 2 sites in India.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 17 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 5 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in India. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact KARTHIK N Dr, MBBS DNB General medicine (+91 9492115369, nalam.karthik8788@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
• Mean change in VAS (Visual analogue scale)scores from baseline to week 12 between the two groups. (time frame: 12 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Jan 2026.