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Central Sensitization in Vitamin D Deficiency

NCT03420378 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 51

Last updated 2018-12-20

No results posted yet for this study

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.

Conditions

  • Vitamin D Deficiency
  • Central Sensitisation

Interventions

DIETARY_SUPPLEMENT

vitamin D

Vitamin D replacement

Sponsors & Collaborators

  • Marmara University

    lead OTHER

Principal Investigators

  • Ozge Kenis Coskun, MD · Marmara Universtiy

Study Design

Allocation
NA
Purpose
SCREENING
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-28
Primary Completion
2018-12-19
Completion
2018-12-19

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03420378 on ClinicalTrials.gov