NCT06004583

C-Reactive Protein/Albumin Ratio and Acne Vulgaris

Relationships Between Disease Severity and The C-Reactive Protein/Albumin Ratio and Various Hematological Parameters in Patients With Acne Vulgaris
Ataturk University·ClinicalTrials.gov·diagnostic testCompleted
View on ClinicalTrials.gov
Study focus
Disease/Condition
Acne Vulgaris
Drug/Device/Intervention
Biochemical blood analysis
Study type
Observational
Intervention type
diagnostic test
Sponsor & location
Primary sponsor
Ataturk University
Location
Erzurum, Turkey
Timeline & enrollment
Phase
N/A
Start date
Jan 05, 2022
End date
May 01, 2023
Enrollment
96 participants
Primary outcome

CRP/albumin ratio

Summary

Objective: Acne vulgaris, an inflammatory disease, was investigated in this study with the
 claim that C-reactive protein (CRP) / albumin ratio and some hematological parameter ratios
 have the potential to be used as inflammatory markers to monitor disease severity and
 prognosis.
 
 Methods: A descriptive cross-sectional study was conducted with two groups of patients aged
 18-65 years, 61 patients diagnosed with acne vulgaris and 35 healthy control patients, and
 routine hemogram and biochemical parameters were compared. The Global Acne Severity Index was
 used to determine the severity of acne vulgaris.

ICD-10 classifications
Acne vulgarisAcneAcne, unspecifiedAcné excoriéeOther acne
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06004583
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06004583 through Pure Global AI's free database. This phase not specified trial is sponsored by Ataturk University and is currently Completed. The study focuses on Acne Vulgaris. Target enrollment is 96 participants.

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