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Clinical Trial Summary

Investigator will examined the diagnostic effect of the endometrial washing by saline. Because this technique more less painful and easier compared to endometrial curettage. Participants will separate into two groups. In study groups before endometrial curettage 5 cc saline infused to the endometrial cavity then aspirate and put into thin prep to examined. After this procedure routine endometrial curettage will be done. In control group only endometrial curettage will be done. Pathologic results of thin prep and curettage will compared.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


NCT number NCT02691715
Study type Interventional
Source Zeynep Kamil Maternity and Pediatric Research and Training Hospital
Contact Mehmet Baki Sentürk, MD
Phone +90 541 773 71 76
Email dr.baki77@gmail.com
Status Recruiting
Phase N/A
Start date January 2016
Completion date June 2016

See also
  Status Clinical Trial Phase
Completed NCT01830192 - REM (Risk Of Endometrial Malignancy) N/A