Vitamin D Treatment for Painful Diabetic Neuropathy
Primary Purpose
Diabetic Neuropathy
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
cholecalciferol
Sponsored by
About this trial
This is an interventional supportive care trial for Diabetic Neuropathy
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.
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
NCT ID
NCT02737423
First Posted
February 1, 2016
Last Updated
April 8, 2016
Sponsor
Baqai Institute of Diabetology and Endocrinology
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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