Endometrial Biopsy as Diagnostic Method for Endometriosis and Endometrioma
NCT ID: NCT01022372
Last Updated: 2011-05-10
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.
UNKNOWN
60 participants
OBSERVATIONAL
2009-11-30
2011-12-31
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.
Assessment of the Uterus Using Ultrasonographic Elastography in Women with Dysmenorrhea
NCT06606834
Pelvic Neuro-Angiogenesis in Deep Endometriosis
NCT06286371
Postoperative Results of Incisional Endometriosis
NCT03900507
Genomic Maps of Endometrial Tissues of Patients With Endometriosis and Healthy Controls
NCT03687398
Endometriosis and Chronic Endometritis
NCT05824507
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
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
control group
Endometrial biopsy
For all the groups
endometriosis group
Endometrial biopsy
For all the groups
endometrioma group
Endometrial biopsy
For all the groups
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Endometrial biopsy
For all the groups
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
17 Years
45 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Selcuk University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
SELCUK UNIVERSITY- MERAM MEDICAL FACULTY
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
The hospital of Meram medical Faculty
Konya, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2009035
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.