MedTrace Logo

3D Ultrasound in Women With Vacuum or Forceps Deliveries

NCT01680731 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 45

Last updated 2014-02-21

No results posted yet for this study

Summary

The purpose of this study is to investigate of the differences in pelvic floor anatomy and function in women who have undergone a vacuum assisted vaginal delivery (VAVD) versus a forceps assisted vaginal delivery (FAVD) using three-dimensional ultrasound imaging. Women within 1-5 years after first delivery who did not have an internal delivery will be included. The total number of subjects is forty. This will include ten primiparous subjects who have undergone vacuum delivery, ten who have undergone forceps delivery, ten who had spontaneous vaginal delivery and ten who have undergone primary elective cesarean section.

Conditions

Sponsors & Collaborators

  • University of Rochester

    lead OTHER

Principal Investigators

  • Tulin Ozcan, MD · University of Rochester

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-10-31
Primary Completion
2013-04-30
Completion
2013-04-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01680731 on ClinicalTrials.gov