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Vitamin D Treatment for Painful Diabetic Neuropathy

Primary Purpose

Diabetic Neuropathy

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
cholecalciferol
Sponsored by
Baqai Institute of Diabetology and Endocrinology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Diabetic Neuropathy

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • All patients with type 1 or type 2 diabetes aged 18 to 80 years
  • Patient has a diagnosis of painful diabetic neuropathy and reports symmetrical painful symptoms in distal extremities for a period of 1-5 years prior to the study, and symptoms were attributable to DPN
  • HbA1c level ≤ 11% at the screening visit were considered eligible to participate in the study.

Exclusion Criteria:

  • Patients with renal impairment or hypo or hyperthyroidism,
  • Patients currently taking vitamin D supplementation or anti - epileptic or anti - tuberculosis medication,
  • Patients with a previous or current history of primary or tertiary hyperparathyroidism, hypercalcemia, psychiatric disorder, alcohol dependency, Hepatitis B or C, HIV infection and peripheral neuropathy due to a non-diabetic cause
  • Pregnant or breast feeding female patients
  • Patients allergic to nuts or any nut products and patients participating in any other interventional research trial were excluded from the study.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    vitamin D

    Arm Description

    single IM dose 600,000 IU of cholecalciferol

    Outcomes

    Primary Outcome Measures

    Improvement in painful diabetic neuropathy by the use of vitamin D Injections (600,000 IU) assessed with the DN4 Neuropathic Pain Diagnostic Questionnaire
    DN4 Neuropathic Pain Diagnostic Questionnaire contains six questions which reflect positive symptoms for pain i.e. question 1, 2, 3, 4, 5 and 10 (sensations of burning, painful cold, electric shocks, tingling, pins & needles and brushing).

    Secondary Outcome Measures

    Improvement in painful diabetic neuropathy by the use of vitamin D Injections (600,000 IU) assessed with the SF-Mac Gill Pain Questionnaire.
    SF-Mac Gill pain questionnaire was evaluated to establish the sensory dimensions of pain which included pain sensations like throbbing, shooting, stabbing, sharp, cramping, gnawing, hot burning, aching, heavy, tender and splitting and effective dimensions of the pain experience which included sensations like tiring-exhausting, sickening, fearful and punishing-cruel.

    Full Information

    First Posted
    February 1, 2016
    Last Updated
    April 8, 2016
    Sponsor
    Baqai Institute of Diabetology and Endocrinology
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02737423
    Brief Title
    Vitamin D Treatment for Painful Diabetic Neuropathy
    Official Title
    Vitamin D for the Treatment of Painful Diabetic Neuropathy
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2016
    Overall Recruitment Status
    Completed
    Study Start Date
    June 2012 (undefined)
    Primary Completion Date
    June 2013 (Actual)
    Study Completion Date
    June 2013 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Baqai Institute of Diabetology and Endocrinology

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The main objective of the study is to assess the effect of vitamin D treatment on painful diabetic neuropathy in Pakistan. This is a prospective study of diabetic patients with a DN score ≥ 4, administered a single dose of 600,000 IU of Vitamin D. All diabetic patients (type 1 and type 2) at the screening visit were considered eligible to participate in the study. The change in painful diabetic neuropathy scores was assessed using DN4 Neuropathic Pain Diagnostic Questionnaire and SF - MPQ for all participants at each visit.
    Detailed Description
    Background Painful diabetic neuropathy (DPN) is common in patients with long-standing diabetes mellitus. The prevalence of neuropathy approaches 50% in those with diabetes for 25 years. Among patients with neuropathy, 11.6% with type 1 diabetes and 32.1% with type 2 diabetes have neuropathic pain. In our recent observational study of a large cohort of diabetic patients from primary care in northwest England (n = 15,692), painful diabetic neuropathy (PDN), assessed using the neuropathy symptom score (NSS) and neuropathy disability score (NDS) (NSS >/=5 and NDS >/=3) was 21%, and the prevalence of painful symptoms (NSS >/=5) was 34%. Despite less neuropathy in South Asians (14%) compared to Europeans (22%) (P < 0.0001), painful symptoms were greater in South Asians (38 vs. 32%, P < 0.0001) and they maintained a 50% increased risk of painful neuropathy symptoms (P < 0.0001). The potential for an association between vitamin D and a beneficial effect on neuropathy is based on experimental data which has shown that vitamin D3 can upregulate NGF and the products of its neuronal target genes resulting in an improvement in experimental diabetic neuropathy. Vitamin D insufficiency has recently been associated with retinopathy and self-reported peripheral neuropathy symptoms even after adjusting for demographic factors, obesity, comorbidities, use of medications for neuropathy and diabetes duration and glycemic control. Of course, there may be some overlap between the symptoms associated with vitamin D deficiency and diabetic neuropathy, which may partly explain the excess painful symptoms we have observed in Asians, particularly as the latter have excess vitamin D deficiency. The preliminary data suggests there is an urgent need to undertake a blinded placebo-controlled randomised trial of vitamin D3 in the treatment of diabetic peripheral neuropathy. Aims: To see the association of Serum Vitamin D3 levels in type 2 diabetic subjects with Painful neuropathy Effect of intervention through injectable Vitamin D3 on Painful diabetic neuropathy Study Design The study is a single centre, single (patient)-blinded, evaluation of injectable cholecalciferol in the treatment of painful diabetic neuropathy. Study Drug: Injectable cholecalciferol (inj. Vitamin D3 600,000 IU). Sample size = 165 type 2 diabetic subjects Recruitment time = 12 weeks Treatment duration = 12 weeks Data Analysis and Statistical Considerations: The normality of the data will be assessed and if the data are severely non-normal, log transformations will be considered. The primary analysis will compare the change from baseline without an alpha adjustment for the multiple comparisons. Comparisons within each treatment group across time will also be considered. The analysis will be performed with Last Observation Carried Forward (LOCF). Assessment during the Treatment Period: Change from baseline in DN4 Change from baseline in SF-MPQ Change from baseline in NeuroQol Change from baseline in serum 25 (OH) D, serum corrected calcium; parathyroid hormone, serum phosphate; serum ALP Change from baseline in HbA1c; fasting glucose; CBC, urea, creatinine, electrolytes, urine DR, fasting lipid profile

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Diabetic Neuropathy

    7. Study Design

    Primary Purpose
    Supportive Care
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    143 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    vitamin D
    Arm Type
    Experimental
    Arm Description
    single IM dose 600,000 IU of cholecalciferol
    Intervention Type
    Drug
    Intervention Name(s)
    cholecalciferol
    Other Intervention Name(s)
    Vitamin D3
    Intervention Description
    Effect of Vitamin D on the symptoms of diabetic neuropathy
    Primary Outcome Measure Information:
    Title
    Improvement in painful diabetic neuropathy by the use of vitamin D Injections (600,000 IU) assessed with the DN4 Neuropathic Pain Diagnostic Questionnaire
    Description
    DN4 Neuropathic Pain Diagnostic Questionnaire contains six questions which reflect positive symptoms for pain i.e. question 1, 2, 3, 4, 5 and 10 (sensations of burning, painful cold, electric shocks, tingling, pins & needles and brushing).
    Time Frame
    5 months
    Secondary Outcome Measure Information:
    Title
    Improvement in painful diabetic neuropathy by the use of vitamin D Injections (600,000 IU) assessed with the SF-Mac Gill Pain Questionnaire.
    Description
    SF-Mac Gill pain questionnaire was evaluated to establish the sensory dimensions of pain which included pain sensations like throbbing, shooting, stabbing, sharp, cramping, gnawing, hot burning, aching, heavy, tender and splitting and effective dimensions of the pain experience which included sensations like tiring-exhausting, sickening, fearful and punishing-cruel.
    Time Frame
    5 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    80 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: All patients with type 1 or type 2 diabetes aged 18 to 80 years Patient has a diagnosis of painful diabetic neuropathy and reports symmetrical painful symptoms in distal extremities for a period of 1-5 years prior to the study, and symptoms were attributable to DPN HbA1c level ≤ 11% at the screening visit were considered eligible to participate in the study. Exclusion Criteria: Patients with renal impairment or hypo or hyperthyroidism, Patients currently taking vitamin D supplementation or anti - epileptic or anti - tuberculosis medication, Patients with a previous or current history of primary or tertiary hyperparathyroidism, hypercalcemia, psychiatric disorder, alcohol dependency, Hepatitis B or C, HIV infection and peripheral neuropathy due to a non-diabetic cause Pregnant or breast feeding female patients Patients allergic to nuts or any nut products and patients participating in any other interventional research trial were excluded from the study.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Abdul Basit, MRCP
    Organizational Affiliation
    Baqai Institute of Diabetology and Endocrinology, Baqai Medical University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

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    Vitamin D Treatment for Painful Diabetic Neuropathy

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