CompletedNot Applicable

Uterine Cavity Assessment and Endometrial Hormonal Receptors in Women With Peri and Post Menopausal Bleeding

Egypt100 participantsStarted 2015-03

Plain-language summary

100 women with abnormal uterine bleeding (peri and postmenopausal) were subjected to transvaginal ultrasound , saline sonohysterography , Diagnostic hysteroscopy and fractional curettage followed by histopathological examination and immunohistochemical analysis for estrogen and progesterone receptors.

Who can participate

Age range45 Years – 65 Years

SexFEMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * women older than 45 years with Abnormal uterine bleeding for more than 3 months duration Exclusion Criteria: * history of hormonal treatment or hormonal contraception within the last 6 months. Women who had used IUD or those had hysteroscopy or fractional curettage done within the last 6 months

What they're measuring

detection of endometrial lesion

Timeframe: 2 days after curretage

Trial details

NCT IDNCT02385747

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2016-02

View on ClinicalTrials.gov More Vaginal Bleeding trials