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The Compatibility of Preoperative Endometrial Biopsies With Postoperative Final Pathology in Endometrial Cancer

NCT04917341 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 960

Last updated 2021-06-08

No results posted yet for this study

Summary

Although there are many studies comparing preoperative and postoperative histological diagnoses in the literature, there are no studies evaluating the compatibility of preoperative histological diagnoses obtained from different centers with postoperative histological diagnoses.Therefore, in our study, we aimed to determine whether preoperative pathological specimens need to be re-evaluated in the referenced hospitals by comparing the compatibility of endometrial specimens in secondary care and tertiary centers with their final pathologies.In our study, we aimed to reveal the under and overdiagnosis rates of the preoperative histological diagnoses of our hospitals compared to the final pathology.

Conditions

  • Endometrial Cancer Stage
  • Gynecologic Cancer

Interventions

DIAGNOSTIC_TEST

re-evaluation of endometrial biopsy samples by a gynecopathologist working at a university hospital

The endometrial biopsy samples taken at the second stage state hospital were re-evaluated by the gynecopathologist working at the university hospital and / or the repeated endometrial biopsy sampling was examined and the evaluation process was carried out in two steps.

Sponsors & Collaborators

  • Eskisehir Osmangazi University

    collaborator OTHER

  • Batman Training and Research Hospital

    lead OTHER_GOV

Principal Investigators

  • Yusuf Cakmak, M.D · Batman education and research hospital

Eligibility

Min Age
40 Years
Max Age
90 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2002-04-12
Primary Completion
2021-04-24
Completion
2021-05-27

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04917341 on ClinicalTrials.gov