At a glance
ClinicalIndex Comparison RecordN/ACompleted· 51 enrolled
Drug / intervention
vitamin Ddietary
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Central Sensitization in Vitamin D Deficiency and Effect of Vitamin D Replacement on Cutaneous Silent Period
In Brief
A clinical study evaluating vitamin D for Vitamin D Deficiency and Central Sensitisation. Completed, enrolled 51 participants across 1 site.
Detailed Summary
The purpose of this study is to investigate the presence of central sensitization in vitamin D deficiency and its effect on cutaneous silent period, pain, and quality of life. The secondary purpose of the study is to investigate whether a change in cutaneous silent period parameters, pain severity and neuropathic sensitization and quality of life after vitamin D replacement.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsVitamin D Deficiency, Central Sensitisation
CountriesTurkey (Türkiye)
Collaborators--
Timeline
N/ACompletedFinished
201820192020202120222023202420252026
Enrollment StartJan 2018
First PostedFeb 2018
Primary CompletionDec 2018
TodayJul 2026
First PostedFeb 5, 2018
Enrollment StartJan 28, 2018
Primary CompletionDec 19, 2018
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 8.4 years ago
Interventions
vitamin Ddietary
Vitamin D replacement