Intrauterine Saline Washing for Detection Endometrial Disease in Patients With Abnormal Uterine Bleeding

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02691715

Enrollment

400

Registered

2016-02-25

Start date

2016-01-31

Completion date

2016-06-30

Last updated

2016-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endometrial Disease

Brief 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.

Interventions

PROCEDUREEndometrial saline plus curettage

PROCEDUREEndometrial curettage

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

DIAGNOSTIC

Masking

NONE

Eligibility

Sex/Gender

FEMALE

Age

35 Years to 80 Years

Healthy volunteers

Yes

Inclusion criteria

* Abnormal uterine bleeding

Exclusion criteria

* Involuntary, under 35 years old,

Design outcomes

Primary

Measure	Time frame	Description
Cervical cytological results according to Bethesda 2003	1 month	for endometrial washing sample
Endometrial hyperplasiz classification according to World Health Organization 2013	1 month	for endometrial curretage sampling

Countries

Turkey (Türkiye)

Contacts

Primary ContactMehmet Baki Şentürk, MD

dr.baki77@gmail.com+90 541 773 71 76

Backup ContactÇetin Kılıççı, MD

cetinkilicci@hotmail.com+90 505 644 94 85

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026