Erdal Pala
Erzurum, 25240, Turkey (Türkiye)
NCT Number: NCT06276829
ABSTRACT Objective: To investigate whether the lactate dehydrogenase to albumin ratio can be used as a parameter to determine disease severity in Behçet's disease, an inflammatory disease, by comparing it to healthy controls.
Patients and Methods: In this retrospective cohort study, patients with Behçet's disease aged 18-69 years who presented to the outpatient clinic between February 2020 and April 2023 and healthy individuals of similar age and gender were enrolled. LDH, albumin levels, and LDH/albumin ratio of both groups were compared. Clinical findings and characteristics of Behçet's patients and disease severity were recorded and analyzed in relation to LDH/albumin ratio.
Looking for future studies?
Notify Me18 year–69 year
All sexes
Observational
Erzurum, 25240, Turkey (Türkiye)
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Patients with Behçet's disease aged 18-69
Exclusion criteria
LDH/Albumin ratios of patient and control groups were recorded.
Time frame: February 2020 and April 2023
Ataturk University
Other
A Convenient Parameter for Predicting Behçet's Disease Severity: Lactate Dehydrogenase/Albumin Ratio
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT01532570
Behcet Syndrome, Behcet's Disease
Chūbu, Japan
View Trial DetailsNCT04065672
Behcet Syndrome, Behcet's Disease
Beijing, China
View Trial DetailsNCT03371095
Behcet Syndrome, Behcet's Disease
Amiens, France
View Trial DetailsNCT01988506
Ankylosing Spondylitis, Ankylosis
Créteil, France
View Trial Details