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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03298100
Other study ID # 3176af
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date September 26, 2017
Est. completion date March 20, 2019

Study information

Verified date December 2018
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

A prospective cohort study to assess RHEA ( recurrent vaginal bleeding, hypertension, endometrial thickness and age) scoring model for prediction of endometrial carcinoma


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 100
Est. completion date March 20, 2019
Est. primary completion date February 28, 2019
Accepts healthy volunteers No
Gender Female
Age group 40 Years and older
Eligibility Inclusion Criteria:

- All postmenopausalwomen with vaginal bleeding and endometrial thickness more than 4 mm

Exclusion Criteria:

- all patients with vaginal bleeding arising from cervical or vaginal or vulval disease or due to hormonal replacement therapy (scheduled bleeding).

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Scoring model
Determining risk factors an calculating the risk score, recurrent vaginal bleeding 3, hypertension 2, age and endometrial thickness 1 for each

Locations

Country Name City State
Egypt Ain Shams University Maternity Hospital Cairo

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Specificity and sensitivity of RHEA scoring mdel Positive and negative productive values, specificity and sensitivity of RHEA scoring model One year
Secondary Variables to increase specificity and sensitivity of the score model Obesity, diabetes mellitus and family history One year
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