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Endometrial Evaluation in Cases of Postmenopausal Bleeding

Cairo University (CU) logo

Cairo University (CU)

Status

Unknown

Conditions

Postmenopausal Bleeding

Treatments

Diagnostic Test: ultrasound

Study type

Observational

Funder types

Other

Identifiers

NCT03847415
endometrial volume

Details and patient eligibility

About

The aim of this prospective observational study is to evaluate abnormal uterine bleeding in postmenopausal women using 3D(dimensional) ultrasound assessment of endometrial volume .Doppler assessment of endometrium and hysteroscopy and to correlate this finding with pathological finding of endometrial biopsy

Full description

Postmenopausal bleeding (PMB) is defined as vaginal bleeding occurring after twelve months of amenorrhoea, in a woman of the age where the menopause can be expected. Hence it does not apply to a young woman, who has had amenorrhoea from anorexia nervosa, or a pregnancy followed by lactation. However, it can apply to younger women following premature ovarian failure or premature menopause, Postmenopausal bleeding is a common problem representing 5% of all gynaecology outpatient attendances. postmenopausal bleeding is usually the first symptom of endometrial cancer and active intervention can lead to its early detection. So, there is need of a diagnostic tool with high accuracy for detection of endometrial pathology in most efficient and least invasive method possible.

Endometrial sampling is the gold standard for diagnosing abnormalities in the endometrial tissues ,however . There is a growing trend to use noninvasive procedures such as TVS, to measure the endometrial thickness, diagnose adenomyosis, endometrial polyps .Another important ability of 3D TVS is volume calculation using the Virtual Organ Computer-aided AnaLysis (VOCAL) even in irregularly shaped structures. This method has been demonstrated to be more accurate than 2D-volume estimation .

• Hysteroscopy has the advantage of directly visualizing the uterine cavity and the endometrium, allowing biopsy to be taken immediately from the suspected abnormality.

Enrollment

100 estimated patients

Sex

Female

Ages

45+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

  • Inclusion Criteria:
  • Women Age > 45 years
  • with postmenopausal uterine bleeding

Exclusion Criteria:

  • Women with bleeding disorders or coagulopathy
  • women with cervical cancer or breast carcinoma .
  • history of tamoxifen intake
  • women with fibroid .

Trial contacts and locations

0

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Central trial contact

Ahmed Aref; Mohamed Reda, M.D

Data sourced from clinicaltrials.gov

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