Progesterone Induced Blocking Factor Expression Levels in Endometrial Cancer Cells.
NCT ID: NCT02852954
Last Updated: 2017-08-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
60 participants
OBSERVATIONAL
2016-08-31
2017-03-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
DNA Analysis of Tumor Tissue Samples From Patients With Diffuse Brain Stem Glioma
NCT00899834
Study of Tissue Samples From Patients With Glioma or Other Brain Tumors
NCT00967200
Immunophenotyping From Blood of Patients With Malignant Gliomas
NCT02022384
MR- PET Guided Biologically Optimised Interstitial Brachytherapy
NCT01391065
Evaluating Serum Sestrin in Leiomyoma Patients
NCT04819633
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
study group1
20 paraffin embedded blocks which was diagnosed endometrial cancer
No interventions assigned to this group
control group
20 paraffin embedded blocks of healthy women
No interventions assigned to this group
study group2
20 paraffin embedded blocks which was diagnosed endometrial hyperplasia
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* diagnosed endometrial hyperplasia
Exclusion Criteria
20 Years
70 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Kayseri Education and Research Hospital
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Erdem Sahin
Director
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2016/405
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.