Uterine Cavity Volume Measuring With Sonohysterography: A New Objective Method

Cavity Clinical Trial

Official title:

Uterine Cavity Volume Measuring With Sonohysterography: A New Objective Method

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03777566
• Other study ID #: mohamed amer
• Status: Recruiting
• Start date: February 10, 2019
• Est. completion date: January 2020

Study information

• Verified date: December 2019
• Source: Ain Shams University
• Contact: Mohamed I Amer, MD
• Phone: 00201001519370
• Email: mohamed_amer810[@]yahoo.com
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

Measuring of uterine cavity volume using sonohysterography will be done in two groups of patients, Group A included 35 patients for home hysterectomy were indicated and group B includes 150 infertile patients in the childbearing age.

Description:

Uterine cavity volume will be measured in group A before and after hysterectomy, and in the group, B will be measured using sonohysterography only using a mathematical method of the sum of a volume of a cone and part of a sphere.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 185
• Est. completion date: January 2020
• Est. primary completion date: December 2019
• Accepts healthy volunteers: No
• Gender: Female
• Age group: N/A and older

Eligibility

Inclusion Criteria:

1. Patients without any gross pathology within the uterus.

2. Patients admitted for hysterectomy.

3. Patients agreed with written consent to participate in the study.

Exclusion Criteria:

1. Virgins.

2. Pregnancy.

3. Systemic blood disease.

4. Any clinical evidence of cervical, uterine or tubal infection.

5. Refusal to undergo saline infusion sonography.

6. Any gross uterine pathology diagnosed clinically or with sonography.

Related Conditions & MeSH terms

• Cavity

Intervention

Diagnostic Test:
• sonohysterography
sonohysterography with measuring the uterine cavity volume

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	calculation of uterine cavity volume with an objective method	measuring uterine cavity volume objectively	one day