Prognosis of METTL-14 in Endometrial Carcinoma
Prognostic Impact of Immunohistochemical Expression of METTL-14 in Endometrial Carcinoma
1 other identifier
observational
50
1 country
1
Brief Summary
- 1.To evaluate immunohistochemical expression of METTL14 in type1 endometrial carcinoma.
- 2.To evaluate the correlation between METTL14 expression and clinicopathological parameters of patients with type 1endometrial carcinoma such as tumor grade, lymhovascular invasion, age of pateints, tumor stage, presence of myometrial invasion and presence of cervical stroma affection.
- 3.To assess correlation of METTL-14 expression with disease free survival and overall survival.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Sep 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 22, 2025
CompletedFirst Posted
Study publicly available on registry
March 6, 2025
CompletedStudy Start
First participant enrolled
September 27, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
October 1, 2026
September 30, 2025
September 1, 2025
10 months
February 22, 2025
September 29, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Evaluation of immunohistochemical Expression of METTL14 in Type 1 Endometrial Carcinoma
Measurement: Percentage of positive METTL14-stained tumor cells using immunohistochemistry (IHC). Unit: Percentage (%). Time Frame: Baseline.
baseline
Study Arms (1)
endometrial carcinoma
Interventions
Eligibility Criteria
endometrial carcinoma
You may qualify if:
- Cases of type1endometrial carcinoma with:
- Hystrectomy operation
- Available full clinical data about patient (age, complaint, findings in clinical examination).
- Full data about previous biopsy and radiology.
- Full data about patient survival, disease progression and history of chemotherapy for three years.
You may not qualify if:
- \. Any case of type 1 endometrial carcinoma with missing clinical, radiologic or follow up data.
- \. Cases with no available H\&E stained slides or formalin fixed paraffin embedded block.
- D\&C.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
AssuitU
Asyut, Egypt
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal investigator
Study Record Dates
First Submitted
February 22, 2025
First Posted
March 6, 2025
Study Start
September 27, 2025
Primary Completion (Estimated)
August 1, 2026
Study Completion (Estimated)
October 1, 2026
Last Updated
September 30, 2025
Record last verified: 2025-09