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Clinical Trial Summary

It is to be achieved that in postmenopausal women through the combination of Hysteroscopy and intraoperative rapid section a positive predictive value (PPV) regarding the objective illness like endometrial cancer or adenomatous hyperplasia of 100% so as a negative predictive value (NPV) of 99%.


Clinical Trial Description

If a patient fulfills the inclusion criteria, the surgeon decides intraoperatively due to the aspect in the hysteroscopy if it is a clearly benign result or if it looks suspicious or malign.

In case of a hysteroscopical benign result the patient will be informed about the result after the operation.

In case of a hysteroscopal suspicious or malignant aspect, the curettement will be sent for a rapid section. If the hysteroscopic result confirms the hysteroscopic suspicion the patient will be informed after the operation and the further treatment can be planned right away. ;


Study Design

Observational Model: Case-Only


Related Conditions & MeSH terms


NCT number NCT01961102
Study type Observational
Source Krankenhaus Barmherzige Schwestern Linz
Contact
Status Completed
Phase N/A
Start date May 2013
Completion date March 2016

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