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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03135353
Other study ID # ED200417
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 20, 2017
Est. completion date November 30, 2018

Study information

Verified date October 2018
Source Woman's Health University Hospital, Egypt
Contact Dina MR Dakhly, MD
Phone 01003498919
Email dinadakhly@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

comparing the efficacy of the 3D saline infusion sonohysterography to the diagnostic office hysteroscopy in the diagnosis of the cause of abnormal uterine bleeding in females during their reproductive age


Recruitment information / eligibility

Status Recruiting
Enrollment 250
Est. completion date November 30, 2018
Est. primary completion date November 25, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 45 Years
Eligibility Inclusion Criteria:

- female aged between 20 and 45 years

- with no medical disorders

- approving to participate in the study

Exclusion Criteria:

- vaginal or cervical lesions

- history or suspicion of PID

- IUD users

- bleeding disorders

- on anticoagulant therapy

- irregular use of oral contraceptive pills

Study Design


Intervention

Device:
3D saline infusion sonohysterography
instillation of saline in the uterine cavity using pediatric foley's catheter, then performing 3D ultrasound scan of the uterus and adenexae
Office Hysteroscopy
an outpatient procedure done to assess the uterine cavity using the office hysteroscopy

Locations

Country Name City State
Egypt Kasr el ainy hospital Cairo

Sponsors (1)

Lead Sponsor Collaborator
Woman's Health University Hospital, Egypt

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary effectiveness of SIS versus office hysteroscopy in the diagnosis of cause of AUB The results of the two procedures would be compared with the operative findings and later histopathological assessment of the specimens 6 months
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