Pilot Study of Vitamin D Screening Use in Peripheral Arterial Disease Patient Over Maximum Distance Walking (First-BLINDOS)
Primary Purpose
Peripheral Arterial Disease
Status
Completed
Phase
Phase 4
Locations
France
Study Type
Interventional
Intervention
Cholecalciferol
Sponsored by
About this trial
This is an interventional treatment trial for Peripheral Arterial Disease focused on measuring peripheral artery disease, Vitamin D
Eligibility Criteria
Inclusion Criteria:
- Patients presenting a Peripheral Arterial Disease (Stage 2)
- Affiliation to the French National healthcare system
- French speaking patients
Exclusion Criteria:
- Pregnancy
- Inability to understand the study goal
- Patients protected by decision of law
Sites / Locations
- CHU Angers
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Patients with Vitamin D deficiency
Arm Description
Patients with Vitamin D deficiency, Administration of Cholecalciferol 2.5 mg (100 000 UI), once a month for 3 months
Outcomes
Primary Outcome Measures
Change of the maximum walking distance on treadmill
the Walking distance will be assessed during a test on a treadmill according to a standardized procedure
Secondary Outcome Measures
Tolerance of vitamin D supplementation during 12 weeks of treatment (period 2)
Prevalence and description of adverse events reported by the patient in a patient book and data collected at the end of treatment
Compliance with Vitamin D supplementation
Recording of vitamin D intake by the patient in a patient booklet and counting of the number of vitamin D boxes in the V2 visit
Full Information
NCT ID
NCT03615833
First Posted
July 30, 2018
Last Updated
September 22, 2020
Sponsor
University Hospital, Angers
1. Study Identification
Unique Protocol Identification Number
NCT03615833
Brief Title
Pilot Study of Vitamin D Screening Use in Peripheral Arterial Disease Patient Over Maximum Distance Walking
Acronym
First-BLINDOS
Official Title
Evaluation of a Strategy for Systematic Screening for Vitamin D Deficiency and Treatment in Case of Deficiency, on the Improvement of the Maximum Walking Distance in Patients With Stage 2 Lower Limb Arterial Disease.
Study Type
Interventional
2. Study Status
Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
March 11, 2019 (Actual)
Primary Completion Date
September 21, 2020 (Actual)
Study Completion Date
September 21, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Angers
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
The prevalence of peripheral arterial disease (PAD) is greater than 15%. PAD is associated with an increased risk of cardiovascular death, coronary heart disease and stroke, with a mortality rate of 5% per year.
Most clinical evidence supports the idea that having normal vitamin D reduces cardiovascular risk. The data suggests that normalizing vitamin D levels would have a significant impact on public health, reduce costs and help control the incidence and prevalence of cardiovascular disease.
There is also a plausible physiological theory, supported by numerous observational studies, that vitamin D supplementation should be effective in improving cardiovascular outcomes, such as blood pressure, arterial stiffness, atherosclerosis, endothelial function, and clinical events.
The investigators hypothesize that routine screening for vitamin D deficiency and supplementation in case of hypovitaminosis D is effective for improving the maximum walking distance after 12 weeks of treatment in stage 2 PAD patients .
Detailed Description
At admission eligible patients are proposed to participate. Written consent is signed after complete oral and written explanation of the protocol is signed. Vitamin D level will be assessed : Patients without vitamin D deficiency will be excluded.
The influence of vitamin D supplementation on the evolution of walking distance in 12 weeks will be studied by comparing the spontaneous evolution of this walking distance, in not supplemented patients (period 1 ), and the evolution under treatment with vitamin D (period 2, afer 3 months ).
The spontaneous evolution of the walking distance will be evaluated by the difference in walking distance observed between the beginning and the end of the first Period (3 months) . The evolution of walking distance under vitamin D treatment will be evaluated by the difference in walking distance between between the beginning and the end of the second Period (3 months).
The duration of participation for a subject is equal to 6 months (2 periods of 3 months )
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Arterial Disease
Keywords
peripheral artery disease, Vitamin D
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
27 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Patients with Vitamin D deficiency
Arm Type
Experimental
Arm Description
Patients with Vitamin D deficiency, Administration of Cholecalciferol 2.5 mg (100 000 UI), once a month for 3 months
Intervention Type
Drug
Intervention Name(s)
Cholecalciferol
Other Intervention Name(s)
Vitamin D
Intervention Description
Cholecalciferol 2.5mg (100 000 UI) , once a month for 3 months
Primary Outcome Measure Information:
Title
Change of the maximum walking distance on treadmill
Description
the Walking distance will be assessed during a test on a treadmill according to a standardized procedure
Time Frame
baseline, 12 weeks and 24 weeks
Secondary Outcome Measure Information:
Title
Tolerance of vitamin D supplementation during 12 weeks of treatment (period 2)
Description
Prevalence and description of adverse events reported by the patient in a patient book and data collected at the end of treatment
Time Frame
24 weeks
Title
Compliance with Vitamin D supplementation
Description
Recording of vitamin D intake by the patient in a patient booklet and counting of the number of vitamin D boxes in the V2 visit
Time Frame
24 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients presenting a Peripheral Arterial Disease (Stage 2)
Affiliation to the French National healthcare system
French speaking patients
Exclusion Criteria:
Pregnancy
Inability to understand the study goal
Patients protected by decision of law
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Samir Henni, MD, PhD
Organizational Affiliation
University Hospital, Angers
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU Angers
City
Angers
ZIP/Postal Code
49933
Country
France
12. IPD Sharing Statement
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Pilot Study of Vitamin D Screening Use in Peripheral Arterial Disease Patient Over Maximum Distance Walking
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