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Relationship of Endometrial Cancer and Serum Soluble L1CAM Level

Completed
Conditions
Endometrium Cancer
Interventions
Diagnostic Test: serum soluble L1CAM (sL1CAM)
Registration Number
NCT04603599
Lead Sponsor
Kocaeli University
Brief Summary

The aim of this study is to evaluate the effect of serum soluble L1CAM (sL1CAM) on the diagnosis and prognosis of endometrial cancer. This prospective randomized controlled trial will be conducted in patients who have undergone endometrial biopsy and whose pathology results are reported as benign endometrial changes, endometrial hyperplasia, or endometrial cancer. The sL1CAM level between groups will be compared. The relationship between prognostic factors and serum sL1CAM will be evaluated in patients with endometrial cancer.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
146
Inclusion Criteria
  • Patients who underwent endometrial biopsy due to abnormal uterine bleeding and whose pathology results were reported as benign endometrial changes, endometrial hyperplasia or endometrial cancer were included in the study. All patients participating in the study signed informed consent.
Exclusion Criteria
  • Patients who did not have consent, received neoadjuvant therapy and who would not have surgery despite endometrial cancer were excluded from the study.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
endometrial cancerserum soluble L1CAM (sL1CAM)-
endometrial hyperplasiaserum soluble L1CAM (sL1CAM)-
benign endometrial changesserum soluble L1CAM (sL1CAM)-
Primary Outcome Measures
NameTimeMethod
serum sL1CAM levelone year
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Merve Demir

🇹🇷

Kocaeli, Turkey

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