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NCT02371811 Clinical Trial

Use of v Care in Abdominal Hysterectomy

Uterine Fibroid Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02371811
Other study ID # m2491
Secondary ID
Status Completed
Phase N/A
First received February 17, 2015
Last updated July 30, 2017
Start date February 2016
Est. completion date July 2017

Study information
Verified date July 2017
Source Ain Shams Maternity Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators use v care during abdominal hysterectomy and evaluate its effect on duration of operation time, surgical complications and vaginal length.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date July 2017
Est. primary completion date July 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- benign causes for hysterectomy

Exclusion Criteria:

- malignant causes for hysterectomy

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• uterine manipulator (v care)

Locations
Country Name City State
Egypt Ain Shams Maternity Hospital Cairo

Sponsors (1)
Lead Sponsor Collaborator
Ain Shams Maternity Hospital

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Vaginal length within 1 week postoperative
Secondary Bladder injury within 1 week postoperative
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