Efficacy of Retrograde Fill Vs Spontaneous Fill to Assess Voiding Function

Completed · Not applicable

Conditions studied: Urinary Retention, Surgery

In brief

Purpose: The purpose of this study is to determine if two different methods of performing a postoperative voiding trial are equivalent in evaluating urinary retention after gynecologic surgery. Participants: The participants in this study will be women who have undergone gynecologic surgery at UNC-Chapel Hill.

Key facts

Study ID

NCT01091844

Run by

University of North Carolina, Chapel Hill

People needed

50

Starts

2009-12-01

Expected to finish

2010-08-01

Last updated by the study team

2010-10-13

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Women undergoing surgical correction of pelvic organ prolapse or urinary incontinence

You may not qualify if…

• Unwillingness to participate in the investigation.
• Inability to give informed consent.
• Known preoperative voiding dysfunction
• Plan for suprapubic catheter placement at time of surgery.
• Age less than 18
• Non-English speaking

Where it is running

• UNC-Chapel Hill — Chapel Hill, North Carolina, United States

Full record on ClinicalTrials.gov

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